A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584502



Internal ID18882783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62448564..62569333hg38UCSC Ensembl
Innerchr20:61023620..61166540hg19UCSC Ensembl
Innerchr20:60457015..60576985hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38120770
hg19142921
hg18119971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060725
Supporting Variants
Samples
Known GenesC20orf166, C20orf166-AS1, GATA5, MIR1-1, MIR133A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584502
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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