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dbVar

Database of genomic structural variation

nsv7026728

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:2,145,410

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: 3910 SVs from 78 studies. See in: genome view

Submitted genomic22,131,232-24,276,641

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7026728	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	22,131,232	24,276,641
nsv7026728	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	22,149,349	24,294,758

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18764297	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
nssv18764297	Submitted genomic		NC_000023.11:g.221 31232_24276641inv	GRCh38 (hg38)		NC_000023.11	ChrX	22,131,232	24,276,641
nssv18764297	Remapped	Perfect	NC_000023.10:g.221 49349_24294758inv	GRCh37.p13	First Pass	NC_000023.10	ChrX	22,149,349	24,294,758

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)
nssv18764297	4.6e-05	10	217391

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