A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759715



Internal ID9981860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126113678..126274679hg38UCSC Ensembl
Innerchr9:128875957..129036958hg19UCSC Ensembl
Innerchr9:127915778..128076779hg18UCSC Ensembl
Innerchr9:125955511..126116512hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38161002
hg19161002
hg18161002
hg17161002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758200
SamplesNA19007
Known Genes
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)esv2759715
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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