A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002653



Internal ID7067768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66186306..66208835hg38UCSC Ensembl
Innerchr9:43166884..43189867hg19UCSC Ensembl
Innerchr9:43156880..43179863hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3822530
hg1922984
hg1822984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586712
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002653
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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