A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14482



Internal ID9977236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28167321..28336066hg38UCSC Ensembl
Innerchr15:28412467..28581212hg19UCSC Ensembl
Innerchr15:26086062..26254807hg18UCSC Ensembl
Innerchr15:26086062..26254807hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38168746
hg19168746
hg18168746
hg17168746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758373
Supporting Variants
SamplesNA19202
Known GenesHERC2
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)essv14482
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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