nsv1154660

Organism: Homo sapiens

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

Variant Calls:43
Validation:Not tested
Clinical Assertions: No
Region Size:22,800

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: 621 SVs from 74 studies. See in: genome view

Remapped(Score: Perfect):122,574,497-122,597,296

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
nsv1154660	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nsv1154660	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812

Variant Call Information

Variant Call ID	Type	Method	Analysis	Copy number
nssv4004531	deletion	SNP array	SNP genotyping analysis	1
nssv4005475	duplication	SNP array	SNP genotyping analysis	3
nssv4005476	deletion	SNP array	SNP genotyping analysis	1
nssv4005477	deletion	SNP array	SNP genotyping analysis	1
nssv4005478	duplication	SNP array	SNP genotyping analysis	3
nssv4005479	deletion	SNP array	SNP genotyping analysis	1
nssv4005480	duplication	SNP array	SNP genotyping analysis	3
nssv4005481	duplication	SNP array	SNP genotyping analysis	3
nssv4005482	duplication	SNP array	SNP genotyping analysis	3
nssv4005483	deletion	SNP array	SNP genotyping analysis	1
nssv4005484	deletion	SNP array	SNP genotyping analysis	1
nssv4005485	duplication	SNP array	SNP genotyping analysis	3
nssv4005486	deletion	SNP array	SNP genotyping analysis	1
nssv4005487	deletion	SNP array	SNP genotyping analysis	1
nssv4005488	deletion	SNP array	SNP genotyping analysis	1
nssv4005489	deletion	SNP array	SNP genotyping analysis	1
nssv4005490	deletion	SNP array	SNP genotyping analysis	1
nssv4005491	deletion	SNP array	SNP genotyping analysis	1
nssv4005492	duplication	SNP array	SNP genotyping analysis	3
nssv4005493	duplication	SNP array	SNP genotyping analysis	4
nssv4005494	duplication	SNP array	SNP genotyping analysis	3
nssv4005495	duplication	SNP array	SNP genotyping analysis	4
nssv4005496	deletion	SNP array	SNP genotyping analysis	1
nssv4005497	duplication	SNP array	SNP genotyping analysis	3
nssv4005498	duplication	SNP array	SNP genotyping analysis	3
nssv4005499	deletion	SNP array	SNP genotyping analysis	1
nssv4005500	deletion	SNP array	SNP genotyping analysis	1
nssv4005501	deletion	SNP array	SNP genotyping analysis	1
nssv4005502	duplication	SNP array	SNP genotyping analysis	4
nssv4005503	deletion	SNP array	SNP genotyping analysis	1
nssv4005504	deletion	SNP array	SNP genotyping analysis	1
nssv4005505	deletion	SNP array	SNP genotyping analysis	0
nssv4005506	deletion	SNP array	SNP genotyping analysis	0
nssv4005507	deletion	SNP array	SNP genotyping analysis	0
nssv4005508	deletion	SNP array	SNP genotyping analysis	0
nssv4005509	deletion	SNP array	SNP genotyping analysis	1
nssv4005510	deletion	SNP array	SNP genotyping analysis	0
nssv4005511	deletion	SNP array	SNP genotyping analysis	1
nssv4005512	duplication	SNP array	SNP genotyping analysis	3
nssv4005513	duplication	SNP array	SNP genotyping analysis	3
nssv4005514	deletion	SNP array	SNP genotyping analysis	1
nssv4005515	deletion	SNP array	SNP genotyping analysis	1
nssv4005516	duplication	SNP array	SNP genotyping analysis	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv4004531	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005475	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005476	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005477	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005478	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005479	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005480	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005481	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005482	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005483	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005484	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005485	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005486	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005487	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005488	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005489	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005490	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005491	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005492	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005493	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005494	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005495	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005496	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005497	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005498	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005499	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005500	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005501	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005502	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005503	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005504	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005505	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005506	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005507	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005508	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005509	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005510	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005511	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005512	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005513	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005514	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005515	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4005516	Remapped	Perfect	NC_000010.11:g.(12 2574497_122582018) _(122591497_122597 296)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,574,497	122,582,018	122,591,497	122,597,296
nssv4004531	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005475	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005476	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005477	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005478	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005479	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005480	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005481	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005482	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005483	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005484	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005485	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005486	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005487	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005488	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005489	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005490	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005491	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005492	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005493	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005494	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005495	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005496	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005497	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005498	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005499	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005500	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005501	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005502	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005503	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005504	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005505	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005506	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005507	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005508	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005509	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005510	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005511	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005512	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005513	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005514	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005515	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812
nssv4005516	Submitted genomic		NC_000010.10:g.(12 4334013_124341534) _(124351013_124356 812)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,334,013	124,341,534	124,351,013	124,356,812

dbVar

Database of genomic structural variation

nsv1154660

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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