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dbVar

Database of genomic structural variation

nsv6131678

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:nsv5553884 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: 76 SVs from 22 studies. See in: genome view

Remapped(Score: Perfect):95,476,539-95,476,539

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131678	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	95,476,539	95,476,539
nsv6131678	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000012.11	Chr12	95,870,315	95,870,315

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17966121	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17966121	Remapped	Perfect	NC_000012.12:g.954 76539_95476540ins?	GRCh38.p12	First Pass	NC_000012.12	Chr12	95,476,539	95,476,539
nssv17966121	Submitted genomic		NC_000012.11:g.958 70315_95870316ins?	GRCh37 (hg19)		NC_000012.11	Chr12	95,870,315	95,870,315

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)
nssv17966121	0.052	313	5996

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