A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759709



Internal ID9635168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109423130..109612496hg38UCSC Ensembl
Innerchr9:112185410..112374776hg19UCSC Ensembl
Innerchr9:111225231..111414597hg18UCSC Ensembl
Innerchr9:109264965..109454331hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38189367
hg19189367
hg18189367
hg17189367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758197
SamplesNA19193
Known GenesPTPN3
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)esv2759709
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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