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

dbVar

Database of genomic structural variation

nsv5668694

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:63,077

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: 498 SVs from 43 studies. See in: genome view

Submitted genomic87,697,526-87,760,602

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5668694	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	87,697,526	87,760,602
nsv5668694	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	86,952,526	87,015,602

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17168545	deletion	HG03732	Sequencing	Sequence alignment	1,582

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17168545	Submitted genomic		NC_000023.11:g.876 97526_87760602delT	GRCh38 (hg38)		NC_000023.11	ChrX	87,697,526	87,760,602
nssv17168545	Remapped	Perfect	NC_000023.10:g.869 52526_87015602delT	GRCh37.p13	First Pass	NC_000023.10	ChrX	86,952,526	87,015,602

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