A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758997



Internal ID9634456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212752087..212833055hg38UCSC Ensembl
Innerchr1:212925429..213006397hg19UCSC Ensembl
Innerchr1:210992052..211073020hg18UCSC Ensembl
Innerchr1:209313824..209394792hg17UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3880969
hg1980969
hg1880969
hg1780969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2756884
SamplesNA12740
Known GenesC1orf227, NSL1, TATDN3
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)esv2758997
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