nsv1156759

Organism: Homo sapiens

Study:nstd97 (Lou et al. 2014)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:47
Validation:Not tested
Clinical Assertions: No
Region Size:22,819

Publication(s):Lou et al. 2014

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: 429 SVs from 62 studies. See in: genome view

Remapped(Score: Perfect):150,588,016-150,610,834

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv1156759	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nsv1156759	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922

Variant Call Information

Variant Call ID	Type	Method	Analysis	Copy number
nssv4019683	deletion	SNP array	SNP genotyping analysis	1
nssv4019684	deletion	SNP array	SNP genotyping analysis	1
nssv4019685	deletion	SNP array	SNP genotyping analysis	0
nssv4019686	deletion	SNP array	SNP genotyping analysis	1
nssv4019687	deletion	SNP array	SNP genotyping analysis	1
nssv4019688	deletion	SNP array	SNP genotyping analysis	1
nssv4019689	deletion	SNP array	SNP genotyping analysis	0
nssv4019690	deletion	SNP array	SNP genotyping analysis	1
nssv4019691	deletion	SNP array	SNP genotyping analysis	1
nssv4019692	duplication	SNP array	SNP genotyping analysis	3
nssv4019693	deletion	SNP array	SNP genotyping analysis	1
nssv4019694	deletion	SNP array	SNP genotyping analysis	1
nssv4019695	deletion	SNP array	SNP genotyping analysis	0
nssv4019696	deletion	SNP array	SNP genotyping analysis	0
nssv4019697	deletion	SNP array	SNP genotyping analysis	1
nssv4019698	deletion	SNP array	SNP genotyping analysis	1
nssv4019699	deletion	SNP array	SNP genotyping analysis	1
nssv4019700	deletion	SNP array	SNP genotyping analysis	0
nssv4019701	deletion	SNP array	SNP genotyping analysis	0
nssv4019702	deletion	SNP array	SNP genotyping analysis	1
nssv4019703	deletion	SNP array	SNP genotyping analysis	0
nssv4019704	deletion	SNP array	SNP genotyping analysis	1
nssv4019705	deletion	SNP array	SNP genotyping analysis	1
nssv4019706	deletion	SNP array	SNP genotyping analysis	1
nssv4019707	deletion	SNP array	SNP genotyping analysis	1
nssv4019708	deletion	SNP array	SNP genotyping analysis	1
nssv4019709	deletion	SNP array	SNP genotyping analysis	1
nssv4019710	deletion	SNP array	SNP genotyping analysis	1
nssv4019711	duplication	SNP array	SNP genotyping analysis	3
nssv4019712	deletion	SNP array	SNP genotyping analysis	1
nssv4019713	deletion	SNP array	SNP genotyping analysis	1
nssv4019714	deletion	SNP array	SNP genotyping analysis	1
nssv4019715	deletion	SNP array	SNP genotyping analysis	1
nssv4019716	deletion	SNP array	SNP genotyping analysis	1
nssv4019717	deletion	SNP array	SNP genotyping analysis	1
nssv4019718	deletion	SNP array	SNP genotyping analysis	1
nssv4019719	deletion	SNP array	SNP genotyping analysis	1
nssv4019720	deletion	SNP array	SNP genotyping analysis	1
nssv4019721	deletion	SNP array	SNP genotyping analysis	1
nssv4019722	deletion	SNP array	SNP genotyping analysis	1
nssv4019723	deletion	SNP array	SNP genotyping analysis	1
nssv4019724	deletion	SNP array	SNP genotyping analysis	0
nssv4019725	deletion	SNP array	SNP genotyping analysis	1
nssv4019726	deletion	SNP array	SNP genotyping analysis	1
nssv4019727	deletion	SNP array	SNP genotyping analysis	0
nssv4019728	deletion	SNP array	SNP genotyping analysis	0
nssv4019729	deletion	SNP array	SNP genotyping analysis	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv4019683	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019684	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019685	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019686	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019687	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019688	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019689	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019690	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019691	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019692	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019693	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019694	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019695	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019696	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019697	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019698	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019699	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019700	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019701	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019702	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019703	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019704	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019705	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019706	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019707	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019708	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019709	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019710	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019711	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019712	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019713	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019714	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019715	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019716	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019717	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019718	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019719	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019720	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019721	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019722	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019723	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019724	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019725	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019726	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019727	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019728	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019729	Remapped	Perfect	NC_000007.14:g.(15 0588016_150588713) _(150604481_150610 834)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	150,588,016	150,588,713	150,604,481	150,610,834
nssv4019683	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019684	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019685	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019686	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019687	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019688	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019689	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019690	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019691	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019692	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)dup	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019693	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019694	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019695	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019696	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019697	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019698	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019699	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019700	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019701	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019702	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019703	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019704	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019705	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019706	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019707	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019708	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019709	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019710	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019711	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)dup	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019712	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019713	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019714	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019715	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019716	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019717	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019718	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019719	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019720	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019721	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019722	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019723	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019724	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019725	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019726	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019727	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019728	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922
nssv4019729	Submitted genomic		NC_000007.13:g.(15 0285104_150285801) _(150301569_150307 922)del	GRCh37 (hg19)		NC_000007.13	Chr7	150,285,104	150,285,801	150,301,569	150,307,922

dbVar

Database of genomic structural variation

nsv1156759

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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

No genotype data were submitted for this variant