A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694928



Internal ID15084894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6133023..6173025hg38UCSC Ensembl
Innerchr7:6172654..6212656hg19UCSC Ensembl
Innerchr7:6139180..6179181hg18UCSC Ensembl
Innerchr7:5945895..5985896hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3840003
hg1940003
hg1840002
hg1740002
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522155
Supporting Variants
Samples
Known GenesCYTH3, USP42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694928
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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