A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732007



Internal ID18683602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:79536661..79582580hg38UCSC Ensembl
Innerchr2:79763787..79809706hg19UCSC Ensembl
Innerchr2:79617295..79663214hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3845920
hg1945920
hg1845920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008702
Supporting Variants
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)nssv3732007
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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