A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759968



Internal ID9982113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111422507..111701647hg38UCSC Ensembl
Innerchr13:112074854..112353994hg19UCSC Ensembl
Innerchr13:110872855..111151995hg18UCSC Ensembl
Innerchr13:110872855..111151995hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38279141
hg19279141
hg18279141
hg17279141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758345
SamplesNA19129
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)esv2759968
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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