A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992827



Internal ID6728788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34380622..34580238hg38UCSC Ensembl
Innerchr15:34672823..34872439hg19UCSC Ensembl
Innerchr15:32460115..32659731hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38199617
hg19199617
hg18199617
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586514
SamplesHuRef
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992827
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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