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dbVar

Database of genomic structural variation

nsv6131014

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:177

Description:nsv5534216 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: 87 SVs from 22 studies. See in: genome view

Remapped(Score: Perfect):90,694,720-90,694,896

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131014	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	90,694,720	90,694,896
nsv6131014	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	91,161,064	91,161,240

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17967422	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17967422	Remapped	Perfect	NC_000014.9:g.9069 4720_90694896ins?	GRCh38.p12	First Pass	NC_000014.9	Chr14	90,694,720	90,694,896
nssv17967422	Submitted genomic		NC_000014.8:g.9116 1064_91161240ins?	GRCh37 (hg19)		NC_000014.8	Chr14	91,161,064	91,161,240

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)
nssv17967422	0.474	3033	6404

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