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

dbVar

Database of genomic structural variation

nsv5653501

Organism: Homo sapiens

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

Variant Calls:2
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: 82 SVs from 29 studies. See in: genome view

Submitted genomic17,050,441-17,050,441

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5653501	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	17,050,441	17,050,441
nsv5653501	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	17,071,988	17,071,988

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17073788	insertion	SAMN00006466	Sequencing	Sequence alignment	4,625
nssv17073789	insertion	SAMN00801888	Sequencing	Sequence alignment	2,004

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17073788	Submitted genomic		NC_000011.10:g.170 50441_17050442ins3 21	GRCh38 (hg38)		NC_000011.10	Chr11	17,050,441	17,050,441
nssv17073789	Submitted genomic		NC_000011.10:g.170 50441_17050442ins9 9	GRCh38 (hg38)		NC_000011.10	Chr11	17,050,441	17,050,441
nssv17073788	Remapped	Perfect	NC_000011.9:g.1707 1988_17071989ins32 1	GRCh37.p13	First Pass	NC_000011.9	Chr11	17,071,988	17,071,988
nssv17073789	Remapped	Perfect	NC_000011.9:g.1707 1988_17071989ins99	GRCh37.p13	First Pass	NC_000011.9	Chr11	17,071,988	17,071,988

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