A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587098



Internal ID7058480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115949956..115950873hg38UCSC Ensembl
Innerchr9:118712235..118713152hg19UCSC Ensembl
Innerchr9:117752056..117752973hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38918
hg19918
hg18918
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995715
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587098
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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