A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758063



Internal ID9980140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77627238..77871113hg38UCSC Ensembl
Innerchr6:78336955..78580830hg19UCSC Ensembl
Innerchr6:78393674..78637549hg18UCSC Ensembl
Innerchr6:78393674..78637549hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38243876
hg19243876
hg18243876
hg17243876
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759446
Supporting Variantsessv14052
SamplesNA18861
Known GenesMEI4
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)esv2758063
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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