esv3833119

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:56
Validation:Not tested
Clinical Assertions: No
Region Size:93,691

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: 660 SVs from 81 studies. See in: genome view

Remapped(Score: Perfect):173,507,638-173,601,328

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3833119	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
esv3833119	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	173,225,428	173,319,118

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv18600042	copy number loss	HG01513	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,385
essv18600043	copy number loss	NA18988	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,938
essv18600044	copy number loss	NA19064	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,315
essv18600045	copy number gain	HG00109	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,672
essv18600046	copy number gain	HG00111	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,151
essv18600047	copy number gain	HG00125	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,034
essv18600048	copy number gain	HG00133	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,432
essv18600049	copy number gain	HG00743	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,757
essv18600050	copy number gain	HG01111	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,414
essv18600051	copy number gain	HG01171	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,424
essv18600052	copy number gain	HG01248	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,370
essv18600053	copy number gain	HG01468	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,777
essv18600054	copy number gain	HG01506	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,694
essv18600055	copy number gain	HG01702	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,332
essv18600056	copy number gain	HG01920	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,547
essv18600057	copy number gain	HG01950	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,545
essv18600058	copy number gain	HG01954	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,032
essv18600059	copy number gain	HG01961	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,329
essv18600060	copy number gain	HG01968	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,970
essv18600061	copy number gain	HG01979	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,599
essv18600062	copy number gain	HG01989	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,773
essv18600063	copy number gain	HG01992	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,376
essv18600064	copy number gain	HG02223	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,201
essv18600065	copy number gain	HG02236	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,543
essv18600066	copy number gain	HG02265	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,313
essv18600067	copy number gain	HG02278	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,119
essv18600068	copy number gain	HG02292	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,911
essv18600069	copy number gain	HG02681	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,767
essv18600070	copy number gain	HG02736	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,693
essv18600071	copy number gain	HG03991	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,102
essv18600072	copy number gain	HG04141	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,802
essv18600073	copy number gain	HG04155	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,496
essv18600074	copy number gain	HG04180	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,561
essv18600075	copy number gain	HG04195	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,469
essv18600076	copy number variation	HG04214	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	3,517
essv18600077	copy number gain	NA11892	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,484
essv18600078	copy number gain	NA12155	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,528
essv18600079	copy number gain	NA12716	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,650
essv18600080	copy number gain	NA19681	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,344
essv18600081	copy number gain	NA19740	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,228
essv18600082	copy number gain	NA19741	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,283
essv18600083	copy number gain	NA19759	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,015
essv18600084	copy number gain	NA19762	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,035
essv18600085	copy number gain	NA19780	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,243
essv18600086	copy number gain	NA19782	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,141
essv18600087	copy number gain	NA20276	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,182
essv18600088	copy number gain	NA20314	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,731
essv18600089	copy number gain	NA20332	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,116
essv18600090	copy number gain	NA20543	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,670
essv18600091	copy number gain	NA20778	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,698
essv18600092	copy number gain	NA20804	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,372
essv18600093	copy number gain	NA20845	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,776
essv18600094	copy number gain	NA20862	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,438
essv18600095	copy number gain	NA20905	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,596
essv18600096	copy number gain	NA21090	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,178
essv18600097	copy number gain	NA21113	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,511

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv18600042	Remapped	Perfect	NC_000003.12:g.173 507638_173601328de l	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600043	Remapped	Perfect	NC_000003.12:g.173 507638_173601328de l	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600044	Remapped	Perfect	NC_000003.12:g.173 507638_173601328de l	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600045	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600046	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600047	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600048	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600049	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600050	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600051	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600052	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600053	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600054	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600055	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600056	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600057	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600058	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600059	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600060	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600061	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600062	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600063	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600064	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600065	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600066	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600067	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600068	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600069	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600070	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600071	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600072	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600073	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600074	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600075	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600076	Remapped	Perfect		GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600077	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600078	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600079	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600080	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600081	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600082	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600083	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600084	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600085	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600086	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600087	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600088	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600089	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600090	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600091	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600092	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600093	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600094	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600095	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600096	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600097	Remapped	Perfect	NC_000003.12:g.173 507638_173601328du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,507,638	173,601,328
essv18600042	Submitted genomic		NC_000003.11:g.173 225428_173319118de l	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600043	Submitted genomic		NC_000003.11:g.173 225428_173319118de l	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600044	Submitted genomic		NC_000003.11:g.173 225428_173319118de l	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600045	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600046	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600047	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600048	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600049	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600050	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600051	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600052	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600053	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600054	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600055	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600056	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600057	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600058	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600059	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600060	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600061	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600062	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600063	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600064	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600065	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600066	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600067	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600068	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600069	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600070	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600071	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600072	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600073	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600074	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600075	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600076	Submitted genomic			GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600077	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600078	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600079	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600080	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600081	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600082	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600083	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600084	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118
essv18600085	Submitted genomic		NC_000003.11:g.173 225428_173319118du p	GRCh37 (hg19)		NC_000003.11	Chr3	173,225,428	173,319,118

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dbVar

Database of genomic structural variation

esv3833119

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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.