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

dbVar

Database of genomic structural variation

nsv5610013

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

Links to Other Resources

Overlapping Genes

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: 140 SVs from 24 studies. See in: genome view

Submitted genomic209,626,459-209,626,459

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5610013	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	209,626,459	209,626,459
nsv5610013	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	209,799,804	209,799,804

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17062629	insertion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17062629	Submitted genomic		NC_000001.11:g.209 626459_209626460in s500	GRCh38 (hg38)		NC_000001.11	Chr1	209,626,459	209,626,459
nssv17062629	Remapped	Perfect	NC_000001.10:g.209 799804_209799805in s500	GRCh37.p13	First Pass	NC_000001.10	Chr1	209,799,804	209,799,804

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

You are here: NCBI