A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760059



Internal ID9982204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95875102..96095471hg38UCSC Ensembl
Innerchr15:96418331..96638700hg19UCSC Ensembl
Innerchr15:94219335..94439704hg18UCSC Ensembl
Innerchr15:94219335..94439704hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38220370
hg19220370
hg18220370
hg17220370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758398
SamplesNA10854
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)esv2760059
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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