A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995430



Internal ID7079853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26905190..26908750hg38UCSC Ensembl
Innerchr22:27301153..27304713hg19UCSC Ensembl
Innerchr22:25631153..25634713hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg383561
hg193561
hg183561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586486
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995430
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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