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

dbVar

Database of genomic structural variation

nsv5661556

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: 238 SVs from 27 studies. See in: genome view

Submitted genomic79,373,367-79,373,367

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5661556	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	79,373,367	79,373,367
nsv5661556	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	79,947,502	79,947,502

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17079929	insertion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17079929	Submitted genomic		NC_000013.11:g.793 73367_79373368ins7 8	GRCh38 (hg38)		NC_000013.11	Chr13	79,373,367	79,373,367
nssv17079929	Remapped	Perfect	NC_000013.10:g.799 47502_79947503ins7 8	GRCh37.p13	First Pass	NC_000013.10	Chr13	79,947,502	79,947,502

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