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dbVar

Database of genomic structural variation

nsv4641621

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:209

Description:nsv4175623 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: 114 SVs from 42 studies. See in: genome view

Remapped(Score: Perfect):7,751,867-7,752,075

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4641621	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	7,751,867	7,752,075
nsv4641621	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	7,793,830	7,794,038

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16159849	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16159849	Remapped	Perfect	NC_000010.11:g.775 1867_7752075del	GRCh38.p12	First Pass	NC_000010.11	Chr10	7,751,867	7,752,075
nssv16159849	Submitted genomic		NC_000010.10:g.779 3830_7794038del	GRCh37 (hg19)		NC_000010.10	Chr10	7,793,830	7,794,038

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)
nssv16159849	0.803	17412	21682

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