A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12336



Internal ID9974859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26199529..26641134hg18UCSC Ensembl
Innerchr15:26199529..26641134hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg18441606
hg17441606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758373
Supporting Variants
SamplesNA19138
Known GenesGOLGA8F, GOLGA8G, HERC2, MIR4509-1, MIR4509-2, MIR4509-3
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)essv12336
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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