A curated catalogue of human genomic structural variation




Variant Details

Variant: essv19992



Internal ID9618104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33289079..33649105hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17360027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758453
Supporting Variants
SamplesNA07048
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)essv19992
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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