A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758584



Internal ID9980661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:115711544..115737957hg38UCSC Ensembl
InnerchrX:114768844..114795257hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3826414
hg1726414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2758885
Supporting Variantsessv2902
SamplesNA18953
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)esv2758584
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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