A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14455



Internal ID9611953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:97305870..97492237hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17186368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757819
Supporting Variants
SamplesNA19201
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)essv14455
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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