A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757358



Internal ID9632817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131414521..131603563hg38UCSC Ensembl
Innerchr9:134289908..134478950hg19UCSC Ensembl
Innerchr9:133279729..133468771hg18UCSC Ensembl
Innerchr9:131319462..131508504hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38189043
hg19189043
hg18189043
hg17189043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759718
Supporting Variantsessv3262
SamplesNA18967
Known GenesPOMT1, PRRC2B, RAPGEF1, SNORD62A, SNORD62B, UCK1
MethodSNP array
AnalysisThe algorithm used to call CNVs using the 500K EA platform was developed to accurately define CNV regions using a large set of reference samples and is described in detail in a separate publication (Komura 2006). The algorithm contains three major parts: 1) Intensity pre-processing using an improved version of Genomic Imbalance Map (GIM) (Ishikawa et al. 2005), including probe selection, noise reduction, normalization, and intensity ratio adjustment based on affinity differences between alleles of a SNP, 2) CNV extraction, which identifies CNVs from all pair-wise comparisons using a modified SW-ARRAY, and 3) A copy number inference step which utilizes signal ratios and SNP information to more precisely define CNV boundaries and the copy number within each region.
PlatformAffymetrix GeneChip Early Access Mapping 500K Set Array (250K_Nsp_SNP)
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)esv2757358
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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