A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758390



Internal ID9980467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81649179..81931728hg38UCSC Ensembl
Innerchr15:81941520..82224069hg19UCSC Ensembl
Innerchr15:79728575..80011124hg18UCSC Ensembl
Innerchr15:79728575..80011124hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38282550
hg19282550
hg18282550
hg17282550
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2760045
Supporting Variantsessv17442
SamplesNA12043
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)esv2758390
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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