A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586833



Internal ID6711529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:39018312..39018821hg38UCSC Ensembl
Innerchr22:39414317..39414826hg19UCSC Ensembl
Innerchr22:37744263..37744772hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38510
hg19510
hg18510
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001536
Supporting Variants
SamplesHuRef
Known GenesAPOBEC3C
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586833
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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