A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758031



Internal ID9633490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179234265..179610528hg38UCSC Ensembl
Innerchr5:178661266..179037529hg19UCSC Ensembl
Innerchr5:178593872..178970135hg18UCSC Ensembl
Innerchr5:178593872..178970135hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38376264
hg19376264
hg18376264
hg17376264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759397
Supporting Variantsessv768, essv892
SamplesNA18956, NA19000
Known GenesADAMTS2, RUFY1
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)esv2758031
Frequency
Sample Size270
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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