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dbVar

Database of genomic structural variation

nsv6131092

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:insertion
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:492

Description:nsv5549670 from Byrska-Bishop et. al 2021. 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: 300 SVs from 50 studies. See in: genome view

Remapped(Score: Perfect):113,025,088-113,025,579

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131092	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	113,025,088	113,025,579
nsv6131092	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	113,679,402	113,679,893

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17966480	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17966480	Remapped	Perfect	NC_000013.11:g.113 025088_113025579in s?	GRCh38.p12	First Pass	NC_000013.11	Chr13	113,025,088	113,025,579
nssv17966480	Submitted genomic		NC_000013.10:g.113 679402_113679893in s?	GRCh37 (hg19)		NC_000013.10	Chr13	113,679,402	113,679,893

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)
nssv17966480	0.426	2168	5090

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