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dbVar

Database of genomic structural variation

nsv4637675

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:261

Description:nsv4074228 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: 107 SVs from 22 studies. See in: genome view

Remapped(Score: Perfect):119,228,588-119,228,848

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4637675	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	119,228,588	119,228,848
nsv4637675	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	118,947,435	118,947,695

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16157186	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16157186	Remapped	Perfect	NC_000003.12:g.119 228588_119228848de l	GRCh38.p12	First Pass	NC_000003.12	Chr3	119,228,588	119,228,848
nssv16157186	Submitted genomic		NC_000003.11:g.118 947435_118947695de l	GRCh37 (hg19)		NC_000003.11	Chr3	118,947,435	118,947,695

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)
nssv16157186	0.094	2027	21650

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