A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759666



Internal ID9981811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10188450..10370398hg38UCSC Ensembl
Innerchr9:10188450..10370398hg19UCSC Ensembl
Innerchr9:10178450..10360398hg18UCSC Ensembl
Innerchr9:10178450..10360398hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38181949
hg19181949
hg18181949
hg17181949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758179
SamplesNA10831
Known GenesPTPRD
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)esv2759666
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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