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dbVar

Database of genomic structural variation

nsv5562677

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:705

Publication(s):Byrska-Bishop 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: 215 SVs from 42 studies. See in: genome view

Submitted genomic806,073-806,777

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5562677	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	806,073	806,777
nsv5562677	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	806,073	806,777

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17043578	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17043578	Submitted genomic		NC_000011.10:g.806 073_806777inv	GRCh38 (hg38)		NC_000011.10	Chr11	806,073	806,777
nssv17043578	Remapped	Perfect	NC_000011.9:g.8060 73_806777inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	806,073	806,777

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)
nssv17043578	<0.001	2	6404

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