A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833890



Internal ID16111073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:131729..287997hg38UCSC Ensembl
Outerchr20:112370..268638hg19UCSC Ensembl
Outerchr20:60370..216638hg18UCSC Ensembl
Outerchr20:60370..216638hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38156269
hg19156269
hg18156269
hg17156269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv65n68
Supporting Variantsnssv1454888, nssv1454889
Samples
Known GenesC20orf96, DEFB126, DEFB127, DEFB128, DEFB129, DEFB132
MethodBAC aCGH
AnalysisExperimental SDs (SDautosome) were calculated for each experiment on the basis of the log2 ratios of the 24,392 reliable clones minus the clones removed because of low signal-to-noise ratio (SNR) or high SD of replicate clone measures (SDclone). Thresholds for determining CNV clones were set at a multiple of the SDautosome value. For each experiment, clones were annotated as uninformative if they were filtered via SNR or SDclone, as a CNV loss if the log2 ratio was less than the negative threshold, as unchanged if the log2 ratio was between the negative and positive thresholds, and as a CNV gain if the log2 ratio was above the positive threshold.
PlatformGPL2616
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833890
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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