A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760058



Internal ID9982203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94923747..95102909hg38UCSC Ensembl
Innerchr15:95466976..95646138hg19UCSC Ensembl
Innerchr15:93267980..93447142hg18UCSC Ensembl
Innerchr15:93267980..93447142hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38179163
hg19179163
hg18179163
hg17179163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758397
SamplesNA18552
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)esv2760058
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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