esv3597711

Organism: Homo sapiens

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

Variant Calls:73
Validation:Not tested
Clinical Assertions: No
Region Size:24,976

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: 589 SVs from 78 studies. See in: genome view

Remapped(Score: Perfect):128,659,814-128,685,447

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3597711	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
esv3597711	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv11138379	deletion	SAMN00004628	Sequencing	Read depth and paired-end mapping	Heterozygous	2,684
essv11138380	deletion	SAMN00004640	Sequencing	Read depth and paired-end mapping	Heterozygous	2,393
essv11138381	deletion	SAMN00006343	Sequencing	Read depth and paired-end mapping	Heterozygous	2,433
essv11138382	deletion	SAMN00004648	Sequencing	Read depth and paired-end mapping	Heterozygous	2,529
essv11138383	deletion	SAMN00004667	Sequencing	Read depth and paired-end mapping	Heterozygous	2,709
essv11138384	deletion	SAMN00004669	Sequencing	Read depth and paired-end mapping	Heterozygous	2,753
essv11138385	deletion	SAMN00006345	Sequencing	Read depth and paired-end mapping	Heterozygous	2,777
essv11138386	deletion	SAMN00016969	Sequencing	Read depth and paired-end mapping	Heterozygous	2,443
essv11138387	deletion	SAMN00009092	Sequencing	Read depth and paired-end mapping	Heterozygous	2,808
essv11138388	deletion	SAMN00006359	Sequencing	Read depth and paired-end mapping	Heterozygous	2,753
essv11138389	deletion	SAMN00009093	Sequencing	Read depth and paired-end mapping	Heterozygous	2,361
essv11138390	deletion	SAMN00009097	Sequencing	Read depth and paired-end mapping	Heterozygous	2,768
essv11138391	deletion	SAMN00006379	Sequencing	Read depth and paired-end mapping	Heterozygous	2,910
essv11138392	deletion	SAMN00009103	Sequencing	Read depth and paired-end mapping	Heterozygous	2,711
essv11138393	deletion	SAMN00009104	Sequencing	Read depth and paired-end mapping	Heterozygous	2,613
essv11138394	deletion	SAMN00006400	Sequencing	Read depth and paired-end mapping	Heterozygous	2,782
essv11138395	deletion	SAMN00006401	Sequencing	Read depth and paired-end mapping	Heterozygous	2,746
essv11138396	deletion	SAMN00006406	Sequencing	Read depth and paired-end mapping	Heterozygous	2,406
essv11138397	deletion	SAMN01091061	Sequencing	Read depth and paired-end mapping	Heterozygous	2,698
essv11138398	deletion	SAMN00009142	Sequencing	Read depth and paired-end mapping	Heterozygous	2,904
essv11138399	deletion	SAMN00009163	Sequencing	Read depth and paired-end mapping	Heterozygous	2,929
essv11138400	deletion	SAMN00009165	Sequencing	Read depth and paired-end mapping	Heterozygous	2,677
essv11138401	deletion	SAMN00009171	Sequencing	Read depth and paired-end mapping	Heterozygous	2,755
essv11138402	deletion	SAMN00009192	Sequencing	Read depth and paired-end mapping	Heterozygous	2,676
essv11138403	deletion	SAMN00009193	Sequencing	Read depth and paired-end mapping	Heterozygous	2,592
essv11138404	deletion	SAMN00009210	Sequencing	Read depth and paired-end mapping	Heterozygous	2,753
essv11138405	deletion	SAMN01091108	Sequencing	Read depth and paired-end mapping	Heterozygous	2,887
essv11138406	deletion	SAMN00014323	Sequencing	Read depth and paired-end mapping	Heterozygous	2,751
essv11138407	deletion	SAMN00014329	Sequencing	Read depth and paired-end mapping	Heterozygous	2,819
essv11138408	deletion	SAMN00014330	Sequencing	Read depth and paired-end mapping	Heterozygous	2,804
essv11138409	deletion	SAMN00014333	Sequencing	Read depth and paired-end mapping	Heterozygous	2,614
essv11138410	deletion	SAMN00014365	Sequencing	Read depth and paired-end mapping	Heterozygous	2,871
essv11138411	deletion	SAMN00014366	Sequencing	Read depth and paired-end mapping	Heterozygous	2,865
essv11138412	deletion	SAMN00014383	Sequencing	Read depth and paired-end mapping	Heterozygous	2,729
essv11138413	deletion	SAMN00014420	Sequencing	Read depth and paired-end mapping	Heterozygous	2,506
essv11138414	deletion	SAMN00016840	Sequencing	Read depth and paired-end mapping	Heterozygous	2,689
essv11138415	deletion	SAMN00016850	Sequencing	Read depth and paired-end mapping	Heterozygous	2,746
essv11138416	deletion	SAMN00249877	Sequencing	Read depth and paired-end mapping	Heterozygous	2,755
essv11138417	deletion	SAMN00255137	Sequencing	Read depth and paired-end mapping	Heterozygous	2,826
essv11138418	deletion	SAMN00263020	Sequencing	Read depth and paired-end mapping	Heterozygous	2,645
essv11138419	deletion	SAMN00263023	Sequencing	Read depth and paired-end mapping	Heterozygous	2,718
essv11138420	deletion	SAMN00779931	Sequencing	Read depth and paired-end mapping	Heterozygous	3,117
essv11138421	deletion	SAMN01091059	Sequencing	Read depth and paired-end mapping	Heterozygous	2,925
essv11138422	deletion	SAMN01036834	Sequencing	Read depth and paired-end mapping	Heterozygous	2,761
essv11138423	deletion	SAMN01091008	Sequencing	Read depth and paired-end mapping	Heterozygous	2,757
essv11138424	deletion	SAMN01096782	Sequencing	Read depth and paired-end mapping	Heterozygous	2,654
essv11138425	deletion	SAMN01096791	Sequencing	Read depth and paired-end mapping	Heterozygous	2,614
essv11138426	deletion	SAMN01761521	Sequencing	Read depth and paired-end mapping	Heterozygous	2,771
essv11138427	deletion	SAMN01091035	Sequencing	Read depth and paired-end mapping	Heterozygous	2,577
essv11138428	deletion	SAMN01096804	Sequencing	Read depth and paired-end mapping	Heterozygous	2,549
essv11138429	deletion	SAMN01761475	Sequencing	Read depth and paired-end mapping	Heterozygous	3,001
essv11138430	deletion	SAMN01761591	Sequencing	Read depth and paired-end mapping	Heterozygous	2,893
essv11138431	deletion	SAMN00800266	Sequencing	Read depth and paired-end mapping	Heterozygous	2,939
essv11138432	deletion	SAMN00800909	Sequencing	Read depth and paired-end mapping	Heterozygous	2,850
essv11138433	deletion	SAMN00000386	Sequencing	Read depth and paired-end mapping	Heterozygous	2,456
essv11138434	deletion	SAMN00801356	Sequencing	Read depth and paired-end mapping	Heterozygous	2,354
essv11138435	deletion	SAMN00801646	Sequencing	Read depth and paired-end mapping	Heterozygous	2,822
essv11138436	deletion	SAMN00801772	Sequencing	Read depth and paired-end mapping	Heterozygous	2,391
essv11138437	deletion	SAMN00801908	Sequencing	Read depth and paired-end mapping	Heterozygous	2,744
essv11138438	deletion	SAMN00007702	Sequencing	Read depth and paired-end mapping	Heterozygous	2,705
essv11138439	deletion	SAMN00007714	Sequencing	Read depth and paired-end mapping	Heterozygous	2,828
essv11138440	deletion	SAMN00007771	Sequencing	Read depth and paired-end mapping	Heterozygous	2,211
essv11138441	deletion	SAMN00004485	Sequencing	Read depth and paired-end mapping	Heterozygous	2,855
essv11138442	deletion	SAMN00001227	Sequencing	Read depth and paired-end mapping	Heterozygous	2,770
essv11138443	deletion	SAMN00001260	Sequencing	Read depth and paired-end mapping	Heterozygous	2,758
essv11138444	deletion	SAMN00001272	Sequencing	Read depth and paired-end mapping	Heterozygous	2,903
essv11138445	deletion	SAMN00001276	Sequencing	Read depth and paired-end mapping	Heterozygous	2,756
essv11138446	deletion	SAMN00001283	Sequencing	Read depth and paired-end mapping	Heterozygous	2,713
essv11138447	deletion	SAMN00004489	Sequencing	Read depth and paired-end mapping	Heterozygous	2,801
essv11138448	deletion	SAMN00007910	Sequencing	Read depth and paired-end mapping	Heterozygous	2,763
essv11138449	deletion	SAMN00007916	Sequencing	Read depth and paired-end mapping	Heterozygous	2,762
essv11138450	deletion	SAMN00007925	Sequencing	Read depth and paired-end mapping	Heterozygous	2,821
essv11138451	deletion	SAMN00004497	Sequencing	Read depth and paired-end mapping	Heterozygous	2,798

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv11138379	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138380	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138381	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138382	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138383	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138384	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138385	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138386	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138387	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138388	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138389	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138390	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138391	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138392	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138393	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138394	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138395	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138396	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138397	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138398	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138399	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138400	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138401	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138402	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138403	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138404	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138405	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138406	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138407	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138408	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138409	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138410	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138411	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138412	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138413	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138414	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138415	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138416	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138417	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138418	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138419	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138420	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138421	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138422	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138423	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138424	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138425	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138426	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138427	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138428	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138429	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138430	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138431	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138432	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138433	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138434	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138435	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138436	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138437	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138438	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138439	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138440	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138441	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138442	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138443	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138444	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138445	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138446	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138447	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138448	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138449	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138450	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138451	Remapped	Perfect	NC_000003.12:g.(12 8659814_128660182) _(128685157_128685 447)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	128,660,182 (-368, +0)	128,685,157 (-0, +290)
essv11138379	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138380	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138381	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138382	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138383	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138384	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138385	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138386	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138387	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138388	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138389	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138390	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138391	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138392	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138393	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138394	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138395	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138396	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138397	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138398	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138399	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138400	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138401	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138402	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138403	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138404	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)
essv11138405	Submitted genomic		NC_000003.11:g.(12 8378657_128379025) _(128404000_128404 290)del	GRCh37 (hg19)		NC_000003.11	Chr3	128,379,025 (-368, +0)	128,404,000 (-0, +290)

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dbVar

Database of genomic structural variation

esv3597711

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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.