A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv818994



Internal ID16407835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105016196..105087057hg38UCSC Ensembl
Innerchr13:105668547..105739408hg19UCSC Ensembl
Innerchr13:104466548..104537409hg18UCSC Ensembl
Innerchr13:104466548..104537409hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3870862
hg1970862
hg1870862
hg1770862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1415597
SamplesNA12236
Known Genes
MethodSNP array
AnalysisAn integrated HMM algorithm was developed and we constructed accurate models for log R Ratio and B Allele Frequency. We developed more realistic models for state transition between different copy number states. PennCNV incorporates the population allele frequency for each SNP and the distance between adjacent SNPs. We incorporated a Bayesian approach into PennCNV to use family information for a posteriori CNV validation and CNV boundary mapping.
PlatformGPL6433
Comments
ReferenceWang_et_al_2007
Pubmed ID17921354
Accession Number(s)nsv818994
Frequency
Sample Size112
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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