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dbVar

Database of genomic structural variation

nsv7071410

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:267,915

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: 1333 SVs from 90 studies. See in: genome view

Submitted genomic107,715,818-107,983,732

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7071410	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	107,715,818	107,983,732
nsv7071410	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	107,586,544	107,854,458

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18744799	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
nssv18744799	Submitted genomic		NC_000011.10:g.107 715818_107983732in v	GRCh38 (hg38)		NC_000011.10	Chr11	107,715,818	107,983,732
nssv18744799	Remapped	Perfect	NC_000011.9:g.1075 86544_107854458inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	107,586,544	107,854,458

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)
nssv18744799	4e-06	1	276268

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