A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833111



Internal ID16110294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:245507..424289hg38UCSC Ensembl
Outerchr16:295506..474289hg19UCSC Ensembl
Outerchr16:235507..414290hg18UCSC Ensembl
Outerchr16:235507..414290hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38178783
hg19178784
hg18178784
hg17178784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv32n68
Supporting Variantsnssv1452117, nssv1452118
Samples
Known GenesARHGDIG, AXIN1, DECR2, ITFG3, LOC100134368, MRPL28, NME4, PDIA2, RGS11, TMEM8A
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)nsv833111
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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