A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694689



Internal ID15084655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5794936..5888325hg38UCSC Ensembl
Innerchr7:5834567..5927956hg19UCSC Ensembl
Innerchr7:5801093..5894482hg18UCSC Ensembl
Innerchr7:5607808..5701197hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3893390
hg1993390
hg1893390
hg1793390
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521919
Supporting Variants
Samples
Known GenesOCM, ZNF815P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694689
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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