A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1444076



Internal ID16094680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:170072762..170230617hg38UCSC Ensembl
Outerchr4:170993913..171151768hg19UCSC Ensembl
Outerchr4:171230488..171388343hg18UCSC Ensembl
Outerchr4:171368643..171526498hg17UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38157856
hg19157856
hg18157856
hg17157856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv830150
Supporting Variants
Samples
Known GenesAADAT
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)nssv1444076
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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