A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2097



Internal ID9619191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60001..407978hg38UCSC Ensembl
Innerchr6:60001..407978hg19UCSC Ensembl
Innerchr6:5001..352978hg18UCSC Ensembl
Innerchr6:5001..352978hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38347978
hg19347978
hg18347978
hg17347978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758034
Supporting Variants
SamplesNA18949
Known GenesDUSP22, IRF4
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)essv2097
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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