A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587227



Internal ID6711923
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995366
Supporting Variants
SamplesHuRef
Known GenesSNX30
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587227
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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