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dbVar

Database of genomic structural variation

nsv4646500

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:301

Description:nsv4259207 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: 126 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):33,081,874-33,082,174

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4646500	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	33,081,874	33,082,174
nsv4646500	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	33,572,780	33,573,080

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16176713	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16176713	Remapped	Perfect	NC_000019.10:g.330 81874_33082174del	GRCh38.p12	First Pass	NC_000019.10	Chr19	33,081,874	33,082,174
nssv16176713	Submitted genomic		NC_000019.9:g.3357 2780_33573080del	GRCh37 (hg19)		NC_000019.9	Chr19	33,572,780	33,573,080

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)
nssv16176713	0.128	2767	21692

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