A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992713



Internal ID7062206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:30670333..30670843hg38UCSC Ensembl
Innerchr22:31066320..31066830hg19UCSC Ensembl
Innerchr22:29396320..29396830hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38511
hg19511
hg18511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587152
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992713
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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