A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060725



Internal ID19149944
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 StatusM
Merged Variantsdgv4344n100
Supporting Variantsnssv3584502
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)nsv1060725
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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