A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759464



Internal ID9981609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:115467214..115640492hg38UCSC Ensembl
Innerchr6:115788378..115961656hg19UCSC Ensembl
Innerchr6:115895071..116068349hg18UCSC Ensembl
Innerchr6:115895071..116068349hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38173279
hg19173279
hg18173279
hg17173279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758075
SamplesNA18632
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)esv2759464
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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