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

dbVar

Database of genomic structural variation

nsv6130769

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:16

Description:nsv5550225 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: 184 SVs from 27 studies. See in: genome view

Remapped(Score: Perfect):36,008,572-36,008,587

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6130769	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	36,008,572	36,008,587
nsv6130769	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000018.9	Chr18	33,588,535	33,588,550

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17958494	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17958494	Remapped	Perfect	NC_000018.10:g.360 08572_36008587ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	36,008,572	36,008,587
nssv17958494	Submitted genomic		NC_000018.9:g.3358 8535_33588550ins?	GRCh37 (hg19)		NC_000018.9	Chr18	33,588,535	33,588,550

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)
nssv17958494	0.014	89	6376

You are here: NCBI