A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757876



Internal ID9633335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:76028139..76118144hg38UCSC Ensembl
Innerchr3:76077290..76167295hg19UCSC Ensembl
Innerchr3:76159980..76249985hg18UCSC Ensembl
Innerchr3:76159980..76249985hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3890006
hg1990006
hg1890006
hg1790006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759157
Supporting Variantsessv21739, essv7286, essv21828
SamplesNA18592, NA12248, NA11839
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)esv2757876
Frequency
Sample Size270
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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