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dbVar

Database of genomic structural variation

nsv7083955

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:561

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: 277 SVs from 32 studies. See in: genome view

Submitted genomic132,806,419-132,806,979

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7083955	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	132,806,419	132,806,979
nsv7083955	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	131,940,447	131,941,007

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18458079	deletion	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18458079	Submitted genomic		NC_000023.11:g.132 806419_132806979de l	GRCh38 (hg38)		NC_000023.11	ChrX	132,806,419	132,806,979
nssv18458079	Remapped	Perfect	NC_000023.10:g.131 940447_131941007de l	GRCh37.p13	First Pass	NC_000023.10	ChrX	131,940,447	131,941,007

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18458079	0.034	7283	216679

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