A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995366



Internal ID6731316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112866635..112867829hg38UCSC Ensembl
Innerchr9:115628915..115630109hg19UCSC Ensembl
Innerchr9:114668736..114669930hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381195
hg191195
hg181195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587227
SamplesHuRef
Known GenesSNX30
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995366
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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