A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1447573



Internal ID16098177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:84171055..84358968hg38UCSC Ensembl
Outerchr1:84636738..84824651hg19UCSC Ensembl
Outerchr1:84409326..84597239hg18UCSC Ensembl
Outerchr1:84348759..84536672hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38187914
hg19187914
hg18187914
hg17187914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv830414
Supporting Variants
Samples
Known GenesPRKACB, SAMD13
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)nssv1447573
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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