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dbVar

Database of genomic structural variation

nsv6832434

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:107

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: 187 SVs from 27 studies. See in: genome view

Submitted genomic156,498,112-156,498,218

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6832434	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	156,498,112	156,498,218
nsv6832434	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	156,290,806	156,290,912

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18722568	duplication	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
nssv18722568	Submitted genomic		NC_000007.14:g.156 498112_156498218du p	GRCh38 (hg38)		NC_000007.14	Chr7	156,498,112	156,498,218
nssv18722568	Remapped	Perfect	NC_000007.13:g.156 290806_156290912du p	GRCh37.p13	First Pass	NC_000007.13	Chr7	156,290,806	156,290,912

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)
nssv18722568	0.003	664	224526

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