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dbVar

Database of genomic structural variation

nsv7020089

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:265,633

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: 487 SVs from 48 studies. See in: genome view

Submitted genomic73,530,622-73,796,254

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7020089	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	73,530,622	73,796,254
nsv7020089	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	72,750,458	73,016,089

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18767231	inversion	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
nssv18767231	Submitted genomic		NC_000023.11:g.735 30622_73796254inv	GRCh38 (hg38)		NC_000023.11	ChrX	73,530,622	73,796,254
nssv18767231	Remapped	Perfect	NC_000023.10:g.727 50458_73016089inv	GRCh37.p13	First Pass	NC_000023.10	ChrX	72,750,458	73,016,089

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)
nssv18767231	1.8e-05	4	222222

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