A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913797



Internal ID15861067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:79752142..79839372hg38UCSC Ensembl
Innerchr2:79979268..80066498hg19UCSC Ensembl
Innerchr2:79832776..79920006hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3887231
hg1987231
hg1887231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582337
Supporting Variants
Samples
Known GenesCTNNA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv913797
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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