A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759697



Internal ID9635156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76750949..77058991hg38UCSC Ensembl
Innerchr9:79365865..79673907hg19UCSC Ensembl
Innerchr9:78555685..78863727hg18UCSC Ensembl
Innerchr9:76595419..76903461hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38308043
hg19308043
hg18308043
hg17308043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758190
SamplesNA18635, NA18632
Known GenesFOXB2, PCA3, PRUNE2
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)esv2759697
Frequency
Sample Size270
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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