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dbVar

Database of genomic structural variation

nsv6810127

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:41

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: 107 SVs from 24 studies. See in: genome view

Submitted genomic150,810,497-150,810,537

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6810127	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	150,810,497	150,810,537
nsv6810127	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	151,131,633	151,131,673

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18522748	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
nssv18522748	Submitted genomic		NC_000006.12:g.150 810497_150810537de l	GRCh38 (hg38)		NC_000006.12	Chr6	150,810,497	150,810,537
nssv18522748	Remapped	Perfect	NC_000006.11:g.151 131633_151131673de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	151,131,633	151,131,673

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)
nssv18522748	0.252	50954	202148

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