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dbVar

Database of genomic structural variation

nsv4638347

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:56,001

Description:nsv4187595 from gnomAD Structural Variants. For a full list of variants now included in nstd186, refer to the mapping file provided here.

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: 365 SVs from 57 studies. See in: genome view

Remapped(Score: Perfect):61,995,848-62,051,848

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4638347	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	61,995,848	62,051,848
nsv4638347	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	45,132,000	45,188,000

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16175196	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16175196	Remapped	Perfect	NC_000009.12:g.619 95848_62051848del	GRCh38.p12	First Pass	NC_000009.12	Chr9	61,995,848	62,051,848
nssv16175196	Submitted genomic		NC_000009.11:g.451 32000_45188000del	GRCh37 (hg19)		NC_000009.11	Chr9	45,132,000	45,188,000

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16175196	0.389	8443	21694

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