A curated catalogue of human genomic structural variation




Variant Details

Variant: essv20939



Internal ID9619157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65888447..66058047hg38UCSC Ensembl
Innerchr15:66180785..66350385hg19UCSC Ensembl
Innerchr15:63967839..64137439hg18UCSC Ensembl
Innerchr15:63967839..64137439hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38169601
hg19169601
hg18169601
hg17169601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758383
Supporting Variants
SamplesNA12801
Known GenesMEGF11, MIR4311, RAB11A
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)essv20939
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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