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dbVar

Database of genomic structural variation

nsv6137723

Organism: Homo sapiens

Study:nstd102 (Clinical Structural Variants)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37, GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:65

Description:Single allele AND not provided

Links to Other Resources

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: 392 SVs from 41 studies. See in: genome view

Submitted genomic679,959-680,023

Variant Region Placement Information

Variant Region ID	Placement Type	Assembly	Assembly Unit	Sequence ID	Chr	Start	Stop
nsv6137723	Submitted genomic	GRCh38 (hg38)	Primary Assembly	NC_000016.10	Chr16	679,959	680,023
nsv6137723	Submitted genomic	GRCh37 (hg19)	Primary Assembly	NC_000016.9	Chr16	729,959	730,023

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv17683560	deletion	Multiple	Multiple	not provided	Benign	ClinVar	RCV001693825.1, VCV001281841.1

Variant Call Placement Information

Variant Call ID	Placement Type	HGVS	Assembly	Sequence ID	Chr	Start	Stop
nssv17683560	Submitted genomic	NC_000016.10:g.679 959_680023del	GRCh38 (hg38)	NC_000016.10	Chr16	679,959	680,023
nssv17683560	Submitted genomic	NC_000016.9:g.7299 59_730023del	GRCh37 (hg19)	NC_000016.9	Chr16	729,959	730,023

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	HGVS	Type	Allele Origin	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv17683560	GRCh37: NC_000016.9:g.729959_730023del, GRCh38: NC_000016.10:g.679959_680023del	deletion	germline	not provided	Benign	ClinVar	RCV001693825.1, VCV001281841.1

No genotype data were submitted for this variant

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