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dbVar

Database of genomic structural variation

nsv5665124

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:127,232

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: 633 SVs from 47 studies. See in: genome view

Submitted genomic127,625,450-127,752,681

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5665124	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	127,625,450	127,752,681
nsv5665124	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	126,759,431	126,886,662

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17165480	deletion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17165480	Submitted genomic		NC_000023.11:g.127 625450_127752681de lA	GRCh38 (hg38)		NC_000023.11	ChrX	127,625,450	127,752,681
nssv17165480	Remapped	Perfect	NC_000023.10:g.126 759431_126886662de lA	GRCh37.p13	First Pass	NC_000023.10	ChrX	126,759,431	126,886,662

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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