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dbVar

Database of genomic structural variation

nsv6804980

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:59

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: 100 SVs from 19 studies. See in: genome view

Submitted genomic151,322,683-151,322,741

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6804980	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	151,322,683	151,322,741
nsv6804980	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	151,643,818	151,643,876

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18711561	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
nssv18711561	Submitted genomic		NC_000006.12:g.151 322683_151322741du p	GRCh38 (hg38)		NC_000006.12	Chr6	151,322,683	151,322,741
nssv18711561	Remapped	Perfect	NC_000006.11:g.151 643818_151643876du p	GRCh37.p13	First Pass	NC_000006.11	Chr6	151,643,818	151,643,876

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)
nssv18711561	0.033	6173	191526

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