A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607683



Internal ID16048406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80633514..80659538hg38UCSC Ensembl
Innerchr7:80262830..80288854hg19UCSC Ensembl
Innerchr7:80100766..80126790hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3826025
hg1926025
hg1826025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155217
SamplesHGDP00632
Known GenesCD36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607683
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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