A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996319



Internal ID7063476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38874401..39063459hg38UCSC Ensembl
Innerchr9:65672409..65858054hg19UCSC Ensembl
Innerchr9:65412229..65597874hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38189059
hg19185646
hg18185646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586226
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996319
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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