A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758195



Internal ID9633654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101877950..102063277hg38UCSC Ensembl
Innerchr9:104640232..104825559hg19UCSC Ensembl
Innerchr9:103680053..103865380hg18UCSC Ensembl
Innerchr9:101719787..101905114hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38185328
hg19185328
hg18185328
hg17185328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759704
Supporting Variantsessv16368
SamplesNA19193
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)esv2758195
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer