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dbVar

Database of genomic structural variation

nsv6131744

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:66

Description:nsv5546627 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: 221 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):45,798,051-45,798,116

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131744	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000021.9	Chr21	45,798,051	45,798,116
nsv6131744	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000021.8	Chr21	47,217,965	47,218,030

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17968222	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17968222	Remapped	Perfect	NC_000021.9:g.4579 8051_45798116ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	45,798,051	45,798,116
nssv17968222	Submitted genomic		NC_000021.8:g.4721 7965_47218030ins?	GRCh37 (hg19)		NC_000021.8	Chr21	47,217,965	47,218,030

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)
nssv17968222	0.034	208	6186

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