A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995869



Internal ID7080179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:81707796..81712723hg38UCSC Ensembl
Outerchr9:84322711..84327638hg19UCSC Ensembl
Outerchr9:83512531..83517458hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg384928
hg194928
hg184928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565651
SamplesHuRef
Known GenesLOC101927502
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995869
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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