A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833930



Internal ID16457799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:16153702..16322118hg38UCSC Ensembl
Outerchr20:16134347..16302763hg19UCSC Ensembl
Outerchr20:16082347..16250763hg18UCSC Ensembl
Outerchr20:16082347..16250763hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38168417
hg19168417
hg18168417
hg17168417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1454990, nssv1454988, nssv1454974, nssv1454992, nssv1454986, nssv1454982, nssv1454973, nssv1454985, nssv1454977, nssv1454991, nssv1454978, nssv1454989, nssv1454993, nssv1454981, nssv1454987, nssv1454983, nssv1454984, nssv1454976, nssv1454975, nssv1454980, nssv1454994, nssv1454979
Samples
Known GenesKIF16B
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)nsv833930
Frequency
Sample Size95
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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