A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830402



Internal ID16454271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:93368195..93511639hg38UCSC Ensembl
Outerchr5:92703901..92847345hg19UCSC Ensembl
Outerchr5:92729657..92873101hg18UCSC Ensembl
Outerchr5:92729657..92873101hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38143445
hg19143445
hg18143445
hg17143445
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1444861, nssv1444864, nssv1444862
Samples
Known GenesNR2F1-AS1
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)nsv830402
Frequency
Sample Size95
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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