A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758074



Internal ID9633533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:114345144..115205793hg38UCSC Ensembl
Innerchr6:114666308..115526957hg19UCSC Ensembl
Innerchr6:114773001..115633650hg18UCSC Ensembl
Innerchr6:114773001..115633650hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38860650
hg19860650
hg18860650
hg17860650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759463
Supporting Variantsessv8749
SamplesNA19092
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)esv2758074
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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