A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758399



Internal ID9980476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97164470..97489514hg38UCSC Ensembl
Innerchr15:97707700..98032744hg19UCSC Ensembl
Innerchr15:95508704..95833748hg18UCSC Ensembl
Innerchr15:95508704..95833748hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38325045
hg19325045
hg18325045
hg17325045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2760060
Supporting Variantsessv6581
SamplesNA18621
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)esv2758399
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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