A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525704



Internal ID15106311
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701864
Samples
Known GenesCD36
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525704
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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