A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759165



Internal ID9981310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103537409..103702318hg38UCSC Ensembl
Innerchr3:103256253..103421162hg19UCSC Ensembl
Innerchr3:104738943..104903852hg18UCSC Ensembl
Innerchr3:104738943..104903852hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38164910
hg19164910
hg18164910
hg17164910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757882
SamplesNA19238
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)esv2759165
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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