A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990797



Internal ID7076928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25780874..25856623hg38UCSC Ensembl
Innerchr20:25761510..25837259hg19UCSC Ensembl
Innerchr20:25709510..25785259hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3875750
hg1975750
hg1875750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586589
SamplesHuRef
Known GenesFAM182B
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990797
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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