A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760041



Internal ID9635500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76878209..77081106hg38UCSC Ensembl
Innerchr15:77170550..77373448hg19UCSC Ensembl
Innerchr15:74957605..75160503hg18UCSC Ensembl
Innerchr15:74957605..75160503hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38202898
hg19202899
hg18202899
hg17202899
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758388
SamplesNA07345
Known GenesPSTPIP1, RCN2, SCAPER, TSPAN3
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)esv2760041
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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