A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001536



Internal ID6713672
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586833
SamplesHuRef
Known GenesAPOBEC3C
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001536
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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