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dbVar

Database of genomic structural variation

nsv6835941

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,771

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: 138 SVs from 46 studies. See in: genome view

Submitted genomic87,679,019-87,681,789

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6835941	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	87,679,019	87,681,789
nsv6835941	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	87,308,335	87,311,105

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18546602	deletion	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
nssv18546602	Submitted genomic		NC_000007.14:g.876 79019_87681789del	GRCh38 (hg38)		NC_000007.14	Chr7	87,679,019	87,681,789
nssv18546602	Remapped	Perfect	NC_000007.13:g.873 08335_87311105del	GRCh37.p13	First Pass	NC_000007.13	Chr7	87,308,335	87,311,105

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)
nssv18546602	0.053	14491	275114

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