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dbVar

Database of genomic structural variation

nsv5666819

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:28,757

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: 230 SVs from 41 studies. See in: genome view

Submitted genomic141,867,716-141,896,472

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5666819	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	141,867,716	141,896,472
nsv5666819	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	142,188,853	142,217,609

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17153023	inversion	HG03486	Optical mapping, Sequencing	Optical mapping, Sequence alignment	4,355

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17153023	Submitted genomic		NC_000006.12:g.141 867716_141896472in v	GRCh38 (hg38)		NC_000006.12	Chr6	141,867,716	141,896,472
nssv17153023	Remapped	Perfect	NC_000006.11:g.142 188853_142217609in v	GRCh37.p13	First Pass	NC_000006.11	Chr6	142,188,853	142,217,609

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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