A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732008



Internal ID18683603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:79822096..79951985hg38UCSC Ensembl
Innerchr2:80049222..80179111hg19UCSC Ensembl
Innerchr2:79902730..80032622hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38129890
hg19129890
hg18129893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000784
Supporting Variants
Samples
Known GenesCTNNA2, MIR8080
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3732008
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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