A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833263



Internal ID16457132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:65997410..66208240hg38UCSC Ensembl
Outerchr16:66031313..66242143hg19UCSC Ensembl
Outerchr16:64588814..64799644hg18UCSC Ensembl
Outerchr16:64588814..64799644hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38210831
hg19210831
hg18210831
hg17210831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1452822
Samples
Known Genes
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)nsv833263
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer