A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8153



Internal ID9977774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26199529..26641134hg18UCSC Ensembl
Innerchr15:26199529..26641134hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg18441606
hg17441606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758373
Supporting Variants
SamplesNA19206
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)essv8153
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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