A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063506



Internal ID19152725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56899344..57089905hg38UCSC Ensembl
Innerchr20:55474400..55664961hg19UCSC Ensembl
Innerchr20:54907807..55098368hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38190562
hg19190562
hg18190562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4333n100
Supporting Variantsnssv3584238, nssv3584239
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063506
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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