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dbVar

Database of genomic structural variation

nsv6707947

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:12,600

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: 177 SVs from 49 studies. See in: genome view

Submitted genomic233,622,201-233,634,800

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6707947	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	233,622,201	233,634,800
nsv6707947	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	234,530,847	234,543,446

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18450679	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
nssv18450679	Submitted genomic		NC_000002.12:g.233 622201_233634800de l	GRCh38 (hg38)		NC_000002.12	Chr2	233,622,201	233,634,800
nssv18450679	Remapped	Perfect	NC_000002.11:g.234 530847_234543446de l	GRCh37.p13	First Pass	NC_000002.11	Chr2	234,530,847	234,543,446

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)
nssv18450679	5.7e-05	14	242830

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