A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758395



Internal ID9633854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90022724..90245993hg38UCSC Ensembl
Innerchr15:90565956..90789225hg19UCSC Ensembl
Innerchr15:88366960..88590229hg18UCSC Ensembl
Innerchr15:88366960..88590229hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38223270
hg19223270
hg18223270
hg17223270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2760054
Supporting Variantsessv15268, essv14606, essv10909, essv11101
SamplesNA19209, NA19094, NA19211, NA19093
Known GenesCIB1, GDPGP1, IDH2, SEMA4B, ZNF710
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)esv2758395
Frequency
Sample Size270
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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