A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757862



Internal ID9633321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24611022..24901435hg38UCSC Ensembl
Innerchr3:24652513..24942926hg19UCSC Ensembl
Innerchr3:24627517..24917930hg18UCSC Ensembl
Innerchr3:24627517..24917930hg17UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38290414
hg19290414
hg18290414
hg17290414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759135
Supporting Variantsessv4819
SamplesNA18620
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)esv2757862
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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