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

dbVar

Database of genomic structural variation

nsv5671846

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:127

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: 413 SVs from 33 studies. See in: genome view

Submitted genomic41,211,739-41,211,865

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5671846	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	41,211,739	41,211,865
nsv5671846	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	41,070,992	41,071,118

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17167775	deletion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17167775	Submitted genomic		NC_000023.11:g.412 11739_41211865delT	GRCh38 (hg38)		NC_000023.11	ChrX	41,211,739	41,211,865
nssv17167775	Remapped	Perfect	NC_000023.10:g.410 70992_41071118delT	GRCh37.p13	First Pass	NC_000023.10	ChrX	41,070,992	41,071,118

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