A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995861



Internal ID6731809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:30246459..30247294hg38UCSC Ensembl
Innerchr22:30642448..30643283hg19UCSC Ensembl
Innerchr22:28972448..28973283hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38836
hg19836
hg18836
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587174
SamplesHuRef
Known GenesLIF
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995861
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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