A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587274



Internal ID7058656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23268397..23269138hg38UCSC Ensembl
Innerchr22:23610584..23611325hg19UCSC Ensembl
Innerchr22:21940584..21941325hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38742
hg19742
hg18742
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994062
Supporting Variants
SamplesHuRef
Known GenesBCR
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587274
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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