Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6131103

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:23

Description:nsv5542308 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: 99 SVs from 16 studies. See in: genome view

Remapped(Score: Perfect):64,989,894-64,989,916

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131103	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	64,989,894	64,989,916
nsv6131103	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	65,282,232	65,282,254

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17964255	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17964255	Remapped	Perfect	NC_000015.10:g.649 89894_64989916ins?	GRCh38.p12	First Pass	NC_000015.10	Chr15	64,989,894	64,989,916
nssv17964255	Submitted genomic		NC_000015.9:g.6528 2232_65282254ins?	GRCh37 (hg19)		NC_000015.9	Chr15	65,282,232	65,282,254

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)
nssv17964255	0.038	239	6324

You are here: NCBI