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dbVar

Database of genomic structural variation

nsv7040762

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:521,368

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: 1677 SVs from 74 studies. See in: genome view

Submitted genomic148,598,948-149,120,315

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7040762	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	148,598,948	149,120,315
nsv7040762	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	148,296,040	148,817,407

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18782052	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
nssv18782052	Submitted genomic		NC_000007.14:g.148 598948_149120315in v	GRCh38 (hg38)		NC_000007.14	Chr7	148,598,948	149,120,315
nssv18782052	Remapped	Perfect	NC_000007.13:g.148 296040_148817407in v	GRCh37.p13	First Pass	NC_000007.13	Chr7	148,296,040	148,817,407

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)
nssv18782052	1.4e-05	4	272838

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