A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758396



Internal ID9633855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:91288620..91497082hg38UCSC Ensembl
Innerchr15:91831850..92040312hg19UCSC Ensembl
Innerchr15:89632854..89841316hg18UCSC Ensembl
Innerchr15:89632854..89841316hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38208463
hg19208463
hg18208463
hg17208463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2760055
Supporting Variantsessv5356
SamplesNA18563
Known GenesSV2B
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)esv2758396
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer