esv3634309

Organism: Homo sapiens

Study:estd214 (1000 Genomes Consortium Phase 3)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:80
Validation:Not tested
Clinical Assertions: No
Region Size:30,071

Publication(s):1000 Genomes Project Consortium et al. 2015

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 383 SVs from 72 studies. See in: genome view

Remapped(Score: Perfect):44,031,335-44,063,405

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3634309	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
esv3634309	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv14999508	deletion	SAMN00006435	Sequencing	Read depth and paired-end mapping	Heterozygous	2,697
essv14999509	deletion	SAMN00006448	Sequencing	Read depth and paired-end mapping	Heterozygous	2,923
essv14999510	deletion	SAMN00006468	Sequencing	Read depth and paired-end mapping	Heterozygous	2,578
essv14999511	deletion	SAMN00006486	Sequencing	Read depth and paired-end mapping	Heterozygous	2,773
essv14999512	deletion	SAMN00006490	Sequencing	Read depth and paired-end mapping	Heterozygous	2,542
essv14999513	deletion	SAMN00006498	Sequencing	Read depth and paired-end mapping	Homozygous	2,728
essv14999514	deletion	SAMN00006504	Sequencing	Read depth and paired-end mapping	Heterozygous	2,702
essv14999515	deletion	SAMN00006529	Sequencing	Read depth and paired-end mapping	Heterozygous	2,283
essv14999516	deletion	SAMN00006573	Sequencing	Read depth and paired-end mapping	Heterozygous	2,632
essv14999517	deletion	SAMN00249887	Sequencing	Read depth and paired-end mapping	Heterozygous	2,781
essv14999518	deletion	SAMN00249890	Sequencing	Read depth and paired-end mapping	Heterozygous	2,692
essv14999519	deletion	SAMN01091062	Sequencing	Read depth and paired-end mapping	Heterozygous	2,669
essv14999520	deletion	SAMN01091106	Sequencing	Read depth and paired-end mapping	Heterozygous	2,886
essv14999521	deletion	SAMN00009245	Sequencing	Read depth and paired-end mapping	Heterozygous	2,611
essv14999522	deletion	SAMN01091109	Sequencing	Read depth and paired-end mapping	Heterozygous	2,856
essv14999523	deletion	SAMN00014335	Sequencing	Read depth and paired-end mapping	Heterozygous	2,734
essv14999524	deletion	SAMN00014350	Sequencing	Read depth and paired-end mapping	Heterozygous	2,736
essv14999525	deletion	SAMN00249676	Sequencing	Read depth and paired-end mapping	Heterozygous	2,663
essv14999526	deletion	SAMN00249903	Sequencing	Read depth and paired-end mapping	Heterozygous	2,724
essv14999527	deletion	SAMN00249820	Sequencing	Read depth and paired-end mapping	Heterozygous	2,679
essv14999528	deletion	SAMN00249837	Sequencing	Read depth and paired-end mapping	Heterozygous	2,698
essv14999529	deletion	SAMN00249848	Sequencing	Read depth and paired-end mapping	Heterozygous	2,567
essv14999530	deletion	SAMN00249700	Sequencing	Read depth and paired-end mapping	Heterozygous	2,666
essv14999531	deletion	SAMN00249703	Sequencing	Read depth and paired-end mapping	Homozygous	2,640
essv14999532	deletion	SAMN00249709	Sequencing	Read depth and paired-end mapping	Heterozygous	2,522
essv14999533	deletion	SAMN00249739	Sequencing	Read depth and paired-end mapping	Heterozygous	2,477
essv14999534	deletion	SAMN00249775	Sequencing	Read depth and paired-end mapping	Heterozygous	2,821
essv14999535	deletion	SAMN00249787	Sequencing	Read depth and paired-end mapping	Heterozygous	2,573
essv14999536	deletion	SAMN00249786	Sequencing	Read depth and paired-end mapping	Heterozygous	2,377
essv14999537	deletion	SAMN00630258	Sequencing	Read depth and paired-end mapping	Heterozygous	2,663
essv14999538	deletion	SAMN00249793	Sequencing	Read depth and paired-end mapping	Heterozygous	2,573
essv14999539	deletion	SAMN00249799	Sequencing	Read depth and paired-end mapping	Heterozygous	2,866
essv14999540	deletion	SAMN00249745	Sequencing	Read depth and paired-end mapping	Heterozygous	2,527
essv14999541	deletion	SAMN00249744	Sequencing	Read depth and paired-end mapping	Heterozygous	2,620
essv14999542	deletion	SAMN00249747	Sequencing	Read depth and paired-end mapping	Heterozygous	2,356
essv14999543	deletion	SAMN00630267	Sequencing	Read depth and paired-end mapping	Heterozygous	2,570
essv14999544	deletion	SAMN00249932	Sequencing	Read depth and paired-end mapping	Heterozygous	2,720
essv14999545	deletion	SAMN01091145	Sequencing	Read depth and paired-end mapping	Heterozygous	2,731
essv14999546	deletion	SAMN00263008	Sequencing	Read depth and paired-end mapping	Heterozygous	2,486
essv14999547	deletion	SAMN00263041	Sequencing	Read depth and paired-end mapping	Heterozygous	2,839
essv14999548	deletion	SAMN00255154	Sequencing	Read depth and paired-end mapping	Heterozygous	2,824
essv14999549	deletion	SAMN00255156	Sequencing	Read depth and paired-end mapping	Heterozygous	2,795
essv14999550	deletion	SAMN00263063	Sequencing	Read depth and paired-end mapping	Heterozygous	2,790
essv14999551	deletion	SAMN01090946	Sequencing	Read depth and paired-end mapping	Heterozygous	2,708
essv14999552	deletion	SAMN00001594	Sequencing	Read depth and paired-end mapping	Heterozygous	2,802
essv14999553	deletion	SAMN00001595	Sequencing	Read depth and paired-end mapping	Heterozygous	2,716
essv14999554	deletion	SAMN00000422	Sequencing	Read depth and paired-end mapping	Heterozygous	2,838
essv14999555	deletion	SAMN00000423	Sequencing	Read depth and paired-end mapping	Heterozygous	2,679
essv14999556	deletion	SAMN00000425	Sequencing	Read depth and paired-end mapping	Heterozygous	2,630
essv14999557	deletion	SAMN00001600	Sequencing	Read depth and paired-end mapping	Heterozygous	2,596
essv14999558	deletion	SAMN00001611	Sequencing	Read depth and paired-end mapping	Heterozygous	2,700
essv14999559	deletion	SAMN00001616	Sequencing	Read depth and paired-end mapping	Heterozygous	2,760
essv14999560	deletion	SAMN00000430	Sequencing	Read depth and paired-end mapping	Heterozygous	2,736
essv14999561	deletion	SAMN00000446	Sequencing	Read depth and paired-end mapping	Homozygous	2,891
essv14999562	deletion	SAMN00000456	Sequencing	Read depth and paired-end mapping	Heterozygous	2,702
essv14999563	deletion	SAMN00000459	Sequencing	Read depth and paired-end mapping	Heterozygous	2,693
essv14999564	deletion	SAMN00000464	Sequencing	Read depth and paired-end mapping	Heterozygous	2,512
essv14999565	deletion	SAMN00000939	Sequencing	Read depth and paired-end mapping	Heterozygous	2,198
essv14999566	deletion	SAMN00000467	Sequencing	Read depth and paired-end mapping	Heterozygous	2,654
essv14999567	deletion	SAMN00001633	Sequencing	Read depth and paired-end mapping	Heterozygous	2,899
essv14999568	deletion	SAMN00000486	Sequencing	Read depth and paired-end mapping	Heterozygous	2,831
essv14999569	deletion	SAMN00001643	Sequencing	Read depth and paired-end mapping	Heterozygous	2,296
essv14999570	deletion	SAMN00000491	Sequencing	Read depth and paired-end mapping	Heterozygous	2,474
essv14999571	deletion	SAMN00000492	Sequencing	Read depth and paired-end mapping	Heterozygous	2,919
essv14999572	deletion	SAMN00001035	Sequencing	Read depth and paired-end mapping	Heterozygous	3,108
essv14999573	deletion	SAMN00000498	Sequencing	Read depth and paired-end mapping	Heterozygous	2,773
essv14999574	deletion	SAMN00000536	Sequencing	Read depth and paired-end mapping	Heterozygous	2,514
essv14999575	deletion	SAMN00000541	Sequencing	Read depth and paired-end mapping	Heterozygous	2,533
essv14999576	deletion	SAMN00000545	Sequencing	Read depth and paired-end mapping	Heterozygous	2,567
essv14999577	deletion	SAMN00007707	Sequencing	Read depth and paired-end mapping	Heterozygous	2,707
essv14999578	deletion	SAMN00007720	Sequencing	Read depth and paired-end mapping	Heterozygous	2,625
essv14999579	deletion	SAMN00007723	Sequencing	Read depth and paired-end mapping	Heterozygous	2,867
essv14999580	deletion	SAMN00007755	Sequencing	Read depth and paired-end mapping	Heterozygous	2,594
essv14999581	deletion	SAMN00004472	Sequencing	Read depth and paired-end mapping	Heterozygous	2,485
essv14999582	deletion	SAMN00007779	Sequencing	Read depth and paired-end mapping	Heterozygous	2,155
essv14999583	deletion	SAMN00007794	Sequencing	Read depth and paired-end mapping	Heterozygous	2,206
essv14999584	deletion	SAMN00006620	Sequencing	Read depth and paired-end mapping	Heterozygous	3,044
essv14999585	deletion	SAMN00007847	Sequencing	Read depth and paired-end mapping	Heterozygous	2,372
essv14999586	deletion	SAMN00007851	Sequencing	Read depth and paired-end mapping	Heterozygous	2,160
essv14999587	deletion	SAMN00001318	Sequencing	Read depth and paired-end mapping	Heterozygous	2,880

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv14999508	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999509	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999510	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999511	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999512	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999513	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999514	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999515	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999516	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999517	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999518	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999519	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999520	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999521	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999522	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999523	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999524	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999525	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999526	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999527	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999528	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999529	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999530	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999531	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999532	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999533	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999534	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999535	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999536	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999537	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999538	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999539	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999540	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999541	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999542	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999543	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999544	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999545	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999546	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999547	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999548	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999549	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999550	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999551	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999552	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999553	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999554	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999555	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999556	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999557	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999558	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999559	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999560	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999561	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999562	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999563	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999564	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999565	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999566	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999567	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999568	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999569	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999570	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999571	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999572	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999573	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999574	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999575	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999576	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999577	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999578	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999579	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999580	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999581	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999582	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999583	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999584	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999585	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999586	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999587	Remapped	Perfect	NC_000014.9:g.(440 31335_44032835)_(4 4061905_44063405)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	44,032,335 (-1000, +500)	44,062,405 (-500, +1000)
essv14999508	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999509	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999510	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999511	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999512	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999513	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999514	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999515	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999516	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999517	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999518	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999519	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999520	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999521	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999522	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999523	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999524	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999525	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999526	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)
essv14999527	Submitted genomic		NC_000014.8:g.(445 00538_44502038)_(4 4531108_44532608)d el	GRCh37 (hg19)		NC_000014.8	Chr14	44,501,538 (-1000, +500)	44,531,608 (-500, +1000)

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dbVar

Database of genomic structural variation

esv3634309

Links to Other Resources

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.