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dbVar

Database of genomic structural variation

nsv5628724

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: 250 SVs from 28 studies. See in: genome view

Submitted genomic125,302,153-125,302,153

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5628724	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	125,302,153	125,302,153
nsv5628724	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	126,314,395	126,314,395

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17153306	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
nssv17153306	Submitted genomic		NC_000008.11:g.125 302153_125302154in s221	GRCh38 (hg38)		NC_000008.11	Chr8	125,302,153	125,302,153
nssv17153306	Remapped	Perfect	NC_000008.10:g.126 314395_126314396in s221	GRCh37.p13	First Pass	NC_000008.10	Chr8	126,314,395	126,314,395

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.

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