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dbVar

Database of genomic structural variation

nsv4642510

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:5,251

Description:nsv4214211 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: 216 SVs from 24 studies. See in: genome view

Remapped(Score: Perfect):110,711,653-110,716,903

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4642510	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	110,711,653	110,716,903
nsv4642510	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	111,364,000	111,369,250

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16164254	duplication	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16164254	Remapped	Perfect	NC_000013.11:g.110 711653_110716903du p	GRCh38.p12	First Pass	NC_000013.11	Chr13	110,711,653	110,716,903
nssv16164254	Submitted genomic		NC_000013.10:g.111 364000_111369250du p	GRCh37 (hg19)		NC_000013.10	Chr13	111,364,000	111,369,250

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)
nssv16164254	0.011	231	20354

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