A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv817895



Internal ID16406736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:50562476..50605697hg38UCSC Ensembl
Innerchr2:50789614..50832835hg19UCSC Ensembl
Innerchr2:50643118..50686339hg18UCSC Ensembl
Innerchr2:50701265..50744486hg17UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3843222
hg1943222
hg1843222
hg1743222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1417577
SamplesNA18972
Known GenesNRXN1
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)nsv817895
Frequency
Sample Size112
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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