A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1447964



Internal ID16098568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114939302..115111871hg38UCSC Ensembl
Outerchr9:117701582..117874150hg19UCSC Ensembl
Outerchr9:116741403..116913971hg18UCSC Ensembl
Outerchr9:114781136..114953704hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38172570
hg19172569
hg18172569
hg17172569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv831696
Supporting Variants
Samples
Known GenesTNC
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)nssv1447964
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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