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dbVar

Database of genomic structural variation

nsv6131053

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:1

Description:nsv5552677 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: 135 SVs from 20 studies. See in: genome view

Remapped(Score: Perfect):78,167,707-78,167,707

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131053	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	78,167,707	78,167,707
nsv6131053	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	76,163,788	76,163,788

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17965161	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17965161	Remapped	Perfect	NC_000017.11:g.781 67707_78167708ins?	GRCh38.p12	First Pass	NC_000017.11	Chr17	78,167,707	78,167,707
nssv17965161	Submitted genomic		NC_000017.10:g.761 63788_76163789ins?	GRCh37 (hg19)		NC_000017.10	Chr17	76,163,788	76,163,788

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)
nssv17965161	0.054	340	6328

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