A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833868



Internal ID16111051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:49848512..49964866hg38UCSC Ensembl
Outerchr19:50351769..50468123hg19UCSC Ensembl
Outerchr19:55043581..55159935hg18UCSC Ensembl
Outerchr19:55043581..55159935hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38116355
hg19116355
hg18116355
hg17116355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv54n68
Supporting Variantsnssv1454847
Samples
Known GenesAKT1S1, ATF5, IL4I1, MIR4749, MIR4750, MIR4751, NUP62, PNKP, PTOV1, PTOV1-AS1, SIGLEC11, TBC1D17
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)nsv833868
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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