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dbVar

Database of genomic structural variation

nsv5667508

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:inversion
Method Type:Optical mapping, Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:51,477

Publication(s):Ebert et al. 2021

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: 604 SVs from 22 studies. See in: genome view

Submitted genomic23,178,077-23,229,553

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5667508	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000024.10	ChrY	23,178,077	23,229,553
nsv5667508	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000024.9	ChrY	25,324,224	25,375,700

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17171152	inversion	Optical mapping, Sequencing	Optical mapping, Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17171152	Submitted genomic		NC_000024.10:g.231 78077_23229553inv	GRCh38 (hg38)		NC_000024.10	ChrY	23,178,077	23,229,553
nssv17171152	Remapped	Perfect	NC_000024.9:g.2532 4224_25375700inv	GRCh37.p13	First Pass	NC_000024.9	ChrY	25,324,224	25,375,700

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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