A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760025



Internal ID9982170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37539368..37680286hg38UCSC Ensembl
Innerchr15:37831569..37972487hg19UCSC Ensembl
Innerchr15:35618861..35759779hg18UCSC Ensembl
Innerchr15:35618861..35759779hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38140919
hg19140919
hg18140919
hg17140919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758377
SamplesNA12814
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)esv2760025
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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