A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759185



Internal ID9981330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144517360..144672545hg38UCSC Ensembl
Innerchr3:144236202..144391387hg19UCSC Ensembl
Innerchr3:145718892..145874077hg18UCSC Ensembl
Innerchr3:145718900..145874085hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38155186
hg19155186
hg18155186
hg17155186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757895
SamplesNA18624
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)esv2759185
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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