A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995606



Internal ID7080029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66944678..66945642hg38UCSC Ensembl
Innerchr11:66712149..66713113hg19UCSC Ensembl
Innerchr11:66468725..66469689hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38965
hg19965
hg18965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586603
SamplesHuRef
Known GenesPC
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995606
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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