A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607684



Internal ID16048407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80657028..80660123hg38UCSC Ensembl
Innerchr7:80286344..80289439hg19UCSC Ensembl
Innerchr7:80124280..80127375hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg383096
hg193096
hg183096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1088536
Samples
Known GenesCD36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607684
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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