A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701864



Internal ID15091830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80574402..80606698hg38UCSC Ensembl
Innerchr7:80203718..80236014hg19UCSC Ensembl
Innerchr7:80041654..80073950hg18UCSC Ensembl
Innerchr7:79848369..79880665hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3832297
hg1932297
hg1832297
hg1732297
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525704
Supporting Variants
Samples
Known GenesCD36
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701864
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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