A curated catalogue of human genomic structural variation




Variant Details

Variant: essv18845



Internal ID9959545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46232533..47972148hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg171739616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758217
Supporting Variants
SamplesNA12751
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)essv18845
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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