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dbVar

Database of genomic structural variation

nsv7068895

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:8,789,977

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: 23031 SVs from 126 studies. See in: genome view

Submitted genomic100,518,680-109,308,656

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7068895	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	100,518,680	109,308,656
nsv7068895	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	100,389,411	109,179,383

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18745091	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
nssv18745091	Submitted genomic		NC_000011.10:g.100 518680_109308656in v	GRCh38 (hg38)		NC_000011.10	Chr11	100,518,680	109,308,656
nssv18745091	Remapped	Perfect	NC_000011.9:g.1003 89411_109179383inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	100,389,411	109,179,383

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)
nssv18745091	4e-06	1	276268

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