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dbVar

Database of genomic structural variation

nsv7072502

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:321,040

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: 752 SVs from 61 studies. See in: genome view

Submitted genomic63,779,608-64,100,647

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7072502	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	63,779,608	64,100,647
nsv7072502	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	64,692,165	65,013,204

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18783524	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
nssv18783524	Submitted genomic		NC_000008.11:g.637 79608_64100647inv	GRCh38 (hg38)		NC_000008.11	Chr8	63,779,608	64,100,647
nssv18783524	Remapped	Perfect	NC_000008.10:g.646 92165_65013204inv	GRCh37.p13	First Pass	NC_000008.10	Chr8	64,692,165	65,013,204

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)
nssv18783524	2.2e-05	6	271434

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