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

dbVar

Database of genomic structural variation

nsv4768878

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:nsv4684560 from Lee et. al 2020. 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: 107 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):86,999,016-86,999,016

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4768878	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	86,999,016	86,999,016
nsv4768878	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	89,613,931	89,613,931

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16252590	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16252590	Remapped	Perfect	NC_000009.12:g.869 99016_86999017ins?	GRCh38.p12	First Pass	NC_000009.12	Chr9	86,999,016	86,999,016
nssv16252590	Submitted genomic		NC_000009.11:g.896 13931_89613932ins?	GRCh37 (hg19)		NC_000009.11	Chr9	89,613,931	89,613,931

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)
nssv16252590	1	1134	1134

You are here: NCBI