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

dbVar

Database of genomic structural variation

nsv4725974

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:nsv4539875 from gnomAD Structural Variants. 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: 131 SVs from 27 studies. See in: genome view

Remapped(Score: Perfect):88,897,514-88,897,514

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4725974	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	88,897,514	88,897,514
nsv4725974	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	89,440,745	89,440,745

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16217553	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16217553	Remapped	Perfect	NC_000015.10:g.888 97514_88897515ins?	GRCh38.p12	First Pass	NC_000015.10	Chr15	88,897,514	88,897,514
nssv16217553	Submitted genomic		NC_000015.9:g.8944 0745_89440746ins?	GRCh37 (hg19)		NC_000015.9	Chr15	89,440,745	89,440,745

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)
nssv16217553	0.111	2398	21692

You are here: NCBI