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dbVar

Database of genomic structural variation

nsv6233833

Organism: Homo sapiens

Study:nstd214 (Naslavsky et al. 2022)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:64

Publication(s):Naslavsky et al. 2022

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: 264 SVs from 26 studies. See in: genome view

Submitted genomic62,907,935-62,907,998

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6233833	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	62,907,935	62,907,998
nsv6233833	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	62,127,405	62,127,468

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17955464	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17955464	Submitted genomic		NC_000023.11:g.629 07935_62907998del	GRCh38 (hg38)		NC_000023.11	ChrX	62,907,935	62,907,998
nssv17955464	Remapped	Perfect	NC_000023.10:g.621 27405_62127468del	GRCh37.p13	First Pass	NC_000023.10	ChrX	62,127,405	62,127,468

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)
nssv17955464	<0.001	1	1775

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