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dbVar

Database of genomic structural variation

nsv4639634

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:50,001

Description:nsv4101232 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: 759 SVs from 77 studies. See in: genome view

Remapped(Score: Perfect):143,991,847-144,041,847

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4639634	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	143,991,847	144,041,847
nsv4639634	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	144,913,000	144,963,000

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16171634	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16171634	Remapped	Perfect	NC_000004.12:g.143 991847_144041847de l	GRCh38.p12	First Pass	NC_000004.12	Chr4	143,991,847	144,041,847
nssv16171634	Submitted genomic		NC_000004.11:g.144 913000_144963000de l	GRCh37 (hg19)		NC_000004.11	Chr4	144,913,000	144,963,000

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)
nssv16171634	0.016	344	21038

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