A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757883



Internal ID9979960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104320533..105096272hg38UCSC Ensembl
Innerchr3:104039377..104815116hg19UCSC Ensembl
Innerchr3:105522067..106297806hg18UCSC Ensembl
Innerchr3:105522067..106297806hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38775740
hg19775740
hg18775740
hg17775740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759166
Supporting Variantsessv2263
SamplesNA18966
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)esv2757883
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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