A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv53n68



Internal ID19006574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49724393..49943224hg38UCSC Ensembl
chr19:50227650..50446481hg19UCSC Ensembl
chr19:54919462..55138293hg18UCSC Ensembl
chr19:54919462..55138293hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38218832
hg19218832
hg18218832
hg17218832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv833867, nsv833866
Samples
Known GenesAKT1S1, AP2A1, ATF5, FUZ, IL4I1, MED25, MIR4749, MIR4750, MIR4751, MIR6799, MIR6800, NUP62, PNKP, PTOV1, PTOV1-AS1, TBC1D17, TSKS
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)dgv53n68
Frequency
Sample Size95
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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