A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012034



Internal ID19101252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:79911119..80064127hg38UCSC Ensembl
Innerchr2:80138245..80291253hg19UCSC Ensembl
Innerchr2:79991756..80144764hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38153009
hg19153009
hg18153009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732009
Samples
Known GenesCTNNA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012034
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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