esv3594848

Organism: Homo sapiens

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

Variant Calls:67
Validation:Not tested
Clinical Assertions: No
Region Size:23,971

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: 950 SVs from 80 studies. See in: genome view

Remapped(Score: Perfect):241,908,017-241,933,214

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3594848	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
esv3594848	Remapped	Good	GRCh38.p12	ALT_REF_LOCI_1	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
esv3594848	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	242,851,168 (-1000, +500)	242,874,365 (-500, +1000)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv10895055	deletion	SAMN00006337	Sequencing	Read depth and paired-end mapping	Heterozygous	2,882
essv10895056	deletion	SAMN00004654	Sequencing	Read depth and paired-end mapping	Heterozygous	2,593
essv10895057	deletion	SAMN00004656	Sequencing	Read depth and paired-end mapping	Heterozygous	2,595
essv10895058	deletion	SAMN00004674	Sequencing	Read depth and paired-end mapping	Heterozygous	2,809
essv10895059	deletion	SAMN00016971	Sequencing	Read depth and paired-end mapping	Heterozygous	2,465
essv10895060	deletion	SAMN00006347	Sequencing	Read depth and paired-end mapping	Heterozygous	2,456
essv10895061	deletion	SAMN00006353	Sequencing	Read depth and paired-end mapping	Heterozygous	2,837
essv10895062	deletion	SAMN00006363	Sequencing	Read depth and paired-end mapping	Heterozygous	2,862
essv10895063	deletion	SAMN00006364	Sequencing	Read depth and paired-end mapping	Heterozygous	2,776
essv10895064	deletion	SAMN00006390	Sequencing	Read depth and paired-end mapping	Heterozygous	2,374
essv10895065	deletion	SAMN00006396	Sequencing	Read depth and paired-end mapping	Heterozygous	2,475
essv10895066	deletion	SAMN00006426	Sequencing	Read depth and paired-end mapping	Heterozygous	2,779
essv10895067	deletion	SAMN00006586	Sequencing	Read depth and paired-end mapping	Heterozygous	2,626
essv10895068	deletion	SAMN00009151	Sequencing	Read depth and paired-end mapping	Heterozygous	2,226
essv10895069	deletion	SAMN00009169	Sequencing	Read depth and paired-end mapping	Heterozygous	2,620
essv10895070	deletion	SAMN00014312	Sequencing	Read depth and paired-end mapping	Heterozygous	2,881
essv10895071	deletion	SAMN00009245	Sequencing	Read depth and paired-end mapping	Heterozygous	2,611
essv10895072	deletion	SAMN00014314	Sequencing	Read depth and paired-end mapping	Heterozygous	2,720
essv10895073	deletion	SAMN01091071	Sequencing	Read depth and paired-end mapping	Heterozygous	2,990
essv10895074	deletion	SAMN01091072	Sequencing	Read depth and paired-end mapping	Heterozygous	2,880
essv10895075	deletion	SAMN01761422	Sequencing	Read depth and paired-end mapping	Heterozygous	2,291
essv10895076	deletion	SAMN00249696	Sequencing	Read depth and paired-end mapping	Heterozygous	2,578
essv10895077	deletion	SAMN00249949	Sequencing	Read depth and paired-end mapping	Heterozygous	2,647
essv10895078	deletion	SAMN00263020	Sequencing	Read depth and paired-end mapping	Heterozygous	2,645
essv10895079	deletion	SAMN01091050	Sequencing	Read depth and paired-end mapping	Heterozygous	2,539
essv10895080	deletion	SAMN01036833	Sequencing	Read depth and paired-end mapping	Heterozygous	2,811
essv10895081	deletion	SAMN01761480	Sequencing	Read depth and paired-end mapping	Heterozygous	2,712
essv10895082	deletion	SAMN01090972	Sequencing	Read depth and paired-end mapping	Heterozygous	2,778
essv10895083	deletion	SAMN01090927	Sequencing	Read depth and paired-end mapping	Heterozygous	2,897
essv10895084	deletion	SAMN01096745	Sequencing	Read depth and paired-end mapping	Heterozygous	2,623
essv10895085	deletion	SAMN01761418	Sequencing	Read depth and paired-end mapping	Heterozygous	2,239
essv10895086	deletion	SAMN01761420	Sequencing	Read depth and paired-end mapping	Heterozygous	2,288
essv10895087	deletion	SAMN01090941	Sequencing	Read depth and paired-end mapping	Heterozygous	2,580
essv10895088	deletion	SAMN01090943	Sequencing	Read depth and paired-end mapping	Heterozygous	2,749
essv10895089	deletion	SAMN01096674	Sequencing	Read depth and paired-end mapping	Heterozygous	2,712
essv10895090	deletion	SAMN01096688	Sequencing	Read depth and paired-end mapping	Heterozygous	2,718
essv10895091	deletion	SAMN01096689	Sequencing	Read depth and paired-end mapping	Heterozygous	2,632
essv10895092	deletion	SAMN01096787	Sequencing	Read depth and paired-end mapping	Heterozygous	2,756
essv10895093	deletion	SAMN01090977	Sequencing	Read depth and paired-end mapping	Heterozygous	2,642
essv10895094	deletion	SAMN01096718	Sequencing	Read depth and paired-end mapping	Heterozygous	2,496
essv10895095	deletion	SAMN01091002	Sequencing	Read depth and paired-end mapping	Heterozygous	2,757
essv10895096	deletion	SAMN01096696	Sequencing	Read depth and paired-end mapping	Heterozygous	2,554
essv10895097	deletion	SAMN01096679	Sequencing	Read depth and paired-end mapping	Heterozygous	2,811
essv10895098	deletion	SAMN01096720	Sequencing	Read depth and paired-end mapping	Heterozygous	2,511
essv10895099	deletion	SAMN01761528	Sequencing	Read depth and paired-end mapping	Heterozygous	2,233
essv10895100	deletion	SAMN01761560	Sequencing	Read depth and paired-end mapping	Heterozygous	2,323
essv10895101	deletion	SAMN01761489	Sequencing	Read depth and paired-end mapping	Heterozygous	2,862
essv10895102	deletion	SAMN01761594	Sequencing	Read depth and paired-end mapping	Heterozygous	2,751
essv10895103	deletion	SAMN00216589	Sequencing	Read depth and paired-end mapping	Heterozygous	2,812
essv10895104	deletion	SAMN00801372	Sequencing	Read depth and paired-end mapping	Heterozygous	2,783
essv10895105	deletion	SAMN00001560	Sequencing	Read depth and paired-end mapping	Heterozygous	2,742
essv10895106	deletion	SAMN00801770	Sequencing	Read depth and paired-end mapping	Heterozygous	2,626
essv10895107	deletion	SAMN00001133	Sequencing	Read depth and paired-end mapping	Heterozygous	3,069
essv10895108	deletion	SAMN00004475	Sequencing	Read depth and paired-end mapping	Heterozygous	2,739
essv10895109	deletion	SAMN00004477	Sequencing	Read depth and paired-end mapping	Heterozygous	2,783
essv10895110	deletion	SAMN00007862	Sequencing	Read depth and paired-end mapping	Heterozygous	2,399
essv10895111	deletion	SAMN00001230	Sequencing	Read depth and paired-end mapping	Heterozygous	2,901
essv10895112	deletion	SAMN00001265	Sequencing	Read depth and paired-end mapping	Heterozygous	2,335
essv10895113	deletion	SAMN00001266	Sequencing	Read depth and paired-end mapping	Heterozygous	2,826
essv10895114	deletion	SAMN00001286	Sequencing	Read depth and paired-end mapping	Heterozygous	2,761
essv10895115	deletion	SAMN00001328	Sequencing	Read depth and paired-end mapping	Heterozygous	2,857
essv10895116	deletion	SAMN00001335	Sequencing	Read depth and paired-end mapping	Heterozygous	2,846
essv10895117	deletion	SAMN00004488	Sequencing	Read depth and paired-end mapping	Heterozygous	2,855
essv10895118	deletion	SAMN00007894	Sequencing	Read depth and paired-end mapping	Heterozygous	2,864
essv10895119	deletion	SAMN00007896	Sequencing	Read depth and paired-end mapping	Heterozygous	2,874
essv10895120	deletion	SAMN00007917	Sequencing	Read depth and paired-end mapping	Heterozygous	2,728
essv10895121	deletion	SAMN00007962	Sequencing	Read depth and paired-end mapping	Heterozygous	2,663

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv10895055	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895056	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895057	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895058	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895059	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895060	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895061	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895062	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895063	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895064	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895065	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895066	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895067	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895068	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895069	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895070	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895071	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895072	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895073	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895074	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895075	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895076	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895077	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895078	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895079	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895080	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895081	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895082	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895083	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895084	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895085	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895086	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895087	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895088	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895089	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895090	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895091	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895092	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895093	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895094	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895095	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895096	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895097	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895098	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895099	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895100	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895101	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895102	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895103	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895104	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895105	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895106	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895107	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895108	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895109	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895110	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895111	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895112	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895113	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895114	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895115	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895116	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895117	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895118	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895119	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895120	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895121	Remapped	Good	NT_187527.1:g.(120 115_121615)_(14458 5_146085)del	GRCh38.p12	Second Pass	NT_187527.1	Chr2\|NT_18 7527.1	121,115 (-1000, +500)	145,085 (-500, +1000)
essv10895055	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895056	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895057	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895058	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895059	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895060	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895061	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895062	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895063	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895064	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895065	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895066	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895067	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895068	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895069	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895070	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895071	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895072	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895073	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895074	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895075	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895076	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895077	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895078	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895079	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895080	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895081	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895082	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895083	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895084	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895085	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895086	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)
essv10895087	Remapped	Perfect	NC_000002.12:g.(24 1908017_241909517) _(241931714_241933 214)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,909,017 (-1000, +500)	241,932,214 (-500, +1000)

Showing 100 of 201

dbVar

Database of genomic structural variation

esv3594848

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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.