A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830229



Internal ID16454098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:21335109..21529992hg38UCSC Ensembl
Outerchr5:21335218..21530101hg19UCSC Ensembl
Outerchr5:21370975..21565858hg18UCSC Ensembl
Outerchr5:21370975..21565858hg17UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38194884
hg19194884
hg18194884
hg17194884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1444343, nssv1444341, nssv1444342
Samples
Known GenesGUSBP1
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)nsv830229
Frequency
Sample Size95
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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