A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759476



Internal ID9634935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143595484..143758839hg38UCSC Ensembl
Innerchr6:143916621..144079976hg19UCSC Ensembl
Innerchr6:143958314..144121669hg18UCSC Ensembl
Innerchr6:143958314..144121669hg17UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38163356
hg19163356
hg18163356
hg17163356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758084
SamplesNA18973
Known GenesPHACTR2
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)esv2759476
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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