A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759928



Internal ID9635387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26426455..26593241hg38UCSC Ensembl
Innerchr13:27000592..27167378hg19UCSC Ensembl
Innerchr13:25898592..26065378hg18UCSC Ensembl
Innerchr13:25898592..26065378hg17UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38166787
hg19166787
hg18166787
hg17166787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758325
SamplesNA18540
Known GenesWASF3
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)esv2759928
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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