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dbVar

Database of genomic structural variation

nsv7058493

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:1,060,863

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: 3013 SVs from 115 studies. See in: genome view

Submitted genomic21,334,980-22,395,842

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7058493	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	21,334,980	22,395,842
nsv7058493	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	21,346,301	22,407,163

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18756417	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
nssv18756417	Submitted genomic		NC_000016.10:g.213 34980_22395842inv	GRCh38 (hg38)		NC_000016.10	Chr16	21,334,980	22,395,842
nssv18756417	Remapped	Perfect	NC_000016.9:g.2134 6301_22407163inv	GRCh37.p13	First Pass	NC_000016.9	Chr16	21,346,301	22,407,163

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)
nssv18756417	1.1e-05	1	273722

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