A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586583



Internal ID6711279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70009981..70075141hg38UCSC Ensembl
Innerchr16:70043884..70109044hg19UCSC Ensembl
Innerchr16:68601385..68666545hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3865161
hg1965161
hg1865161
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv987821
Supporting Variants
SamplesHuRef
Known GenesMIR1972-1, MIR1972-2, PDXDC2P
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586583
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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