esv3875353

Organism: Homo sapiens

Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:37
Validation:Not tested
Clinical Assertions: No
Region Size:11,869

Publication(s):1000 Genomes Consortium Phase 3 Integrated SV

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: 276 SVs from 53 studies. See in: genome view

Remapped(Score: Perfect):61,394,545-61,406,830

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3875353	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
esv3875353	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv23774179	deletion	HG00103	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,063
essv23774180	deletion	HG00117	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,398
essv23774181	deletion	HG00178	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,406
essv23774182	deletion	HG00250	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,391
essv23774183	deletion	HG00267	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,486
essv23774184	deletion	HG00311	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,551
essv23774185	deletion	HG00361	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,647
essv23774186	deletion	HG00364	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,292
essv23774187	deletion	HG00379	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,279
essv23774188	deletion	HG01066	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,614
essv23774189	deletion	HG01259	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,642
essv23774190	deletion	HG01281	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,331
essv23774191	deletion	HG01378	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,179
essv23774192	deletion	HG01432	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,051
essv23774193	deletion	HG01485	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,068
essv23774194	deletion	HG01495	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,329
essv23774195	deletion	HG01607	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,053
essv23774196	deletion	HG01766	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,435
essv23774197	deletion	HG02283	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,207
essv23774198	deletion	HG03781	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,412
essv23774199	deletion	HG04171	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,431
essv23774200	deletion	HG04195	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,469
essv23774201	deletion	NA11893	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,664
essv23774202	deletion	NA11894	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,394
essv23774203	deletion	NA12045	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,512
essv23774204	deletion	NA12046	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,306
essv23774205	deletion	NA12399	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,513
essv23774206	deletion	NA12842	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,543
essv23774207	deletion	NA12873	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,054
essv23774208	deletion	NA20332	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,116
essv23774209	deletion	NA20516	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,702
essv23774210	deletion	NA20525	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,649
essv23774211	deletion	NA20534	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,666
essv23774212	deletion	NA20756	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,376
essv23774213	deletion	NA20809	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,667
essv23774214	deletion	NA20822	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,490
essv23774215	deletion	NA20885	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,591

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv23774179	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774180	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774181	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774182	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774183	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774184	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774185	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774186	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774187	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774188	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774189	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774190	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774191	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774192	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774193	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774194	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774195	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774196	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774197	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774198	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774199	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774200	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774201	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774202	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774203	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774204	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774205	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774206	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774207	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774208	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774209	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774210	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774211	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774212	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774213	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774214	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774215	Remapped	Perfect	NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	61,394,751 (-206, +0)	61,406,619 (-0, +211)
essv23774179	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774180	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774181	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774182	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774183	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774184	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774185	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774186	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774187	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774188	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774189	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774190	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774191	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774192	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774193	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774194	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774195	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774196	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774197	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774198	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774199	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774200	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774201	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774202	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774203	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774204	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774205	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774206	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774207	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774208	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774209	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774210	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774211	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774212	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774213	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774214	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)
essv23774215	Submitted genomic		NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el	GRCh37 (hg19)		NC_000015.9	Chr15	61,686,950 (-206, +0)	61,698,818 (-0, +211)

dbVar

Database of genomic structural variation

esv3875353

Links to Other Resources

Genome View

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.