A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1444772



Internal ID16442062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:81898350..81949932hg38UCSC Ensembl
Outerchr5:81194169..81245751hg19UCSC Ensembl
Outerchr5:81229925..81281507hg18UCSC Ensembl
Outerchr5:81229925..81281507hg17UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3851583
hg1951583
hg1851583
hg1751583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv830363
Supporting Variants
Samples
Known Genes
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)nssv1444772
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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