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dbVar

Database of genomic structural variation

nsv4656337

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:27,209

Description:esv3870513 from 1000 Genomes Consortium Phase 3 Integrated SV. 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: 401 SVs from 61 studies. See in: genome view

Remapped(Score: Perfect):57,292,518-57,319,726

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4656337	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	57,292,518	57,319,726
nsv4656337	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	57,866,652	57,893,860

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16192255	copy number loss	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16192255	Remapped	Perfect	NC_000013.11:g.572 92518_57319726del	GRCh38.p12	First Pass	NC_000013.11	Chr13	57,292,518	57,319,726
nssv16192255	Submitted genomic		NC_000013.10:g.578 66652_57893860del	GRCh37 (hg19)		NC_000013.10	Chr13	57,866,652	57,893,860

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)
nssv16192255	0.015	73	5008

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