A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759606



Internal ID9635065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25411509..25564618hg38UCSC Ensembl
Innerchr8:25269025..25422134hg19UCSC Ensembl
Innerchr8:25324942..25478051hg18UCSC Ensembl
Innerchr8:25324942..25478051hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38153110
hg19153110
hg18153110
hg17153110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758153
SamplesNA19007
Known GenesCDCA2, DOCK5, GNRH1, KCTD9
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)esv2759606
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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