A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859071



Internal ID15806341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:66876182..66938470hg38UCSC Ensembl
Innerchr16:66910085..66972373hg19UCSC Ensembl
Innerchr16:65467586..65529874hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3862289
hg1962289
hg1862289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572904
Supporting Variants
Samples
Known GenesCDH16, CES2, FAM96B, PDP2, RRAD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv859071
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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