A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833848



Internal ID16111031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:45457372..45644939hg38UCSC Ensembl
Outerchr19:45960630..46148197hg19UCSC Ensembl
Outerchr19:50652470..50840037hg18UCSC Ensembl
Outerchr19:50652470..50840037hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38187568
hg19187568
hg18187568
hg17187568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1454753, nssv1454754
Samples
Known GenesC19orf83, EML2, FOSB, GPR4, MIR330, OPA3, PPM1N, RTN2, VASP
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)nsv833848
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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