A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759703



Internal ID9635162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87403812..87810065hg38UCSC Ensembl
Innerchr9:90018727..90424980hg19UCSC Ensembl
Innerchr9:89208547..89614800hg18UCSC Ensembl
Innerchr9:87248281..87654534hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38406254
hg19406254
hg18406254
hg17406254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758194
SamplesNA19154
Known GenesCTSL, CTSL3P, DAPK1
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)esv2759703
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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