A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832699



Internal ID16109882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:100951779..101142880hg38UCSC Ensembl
Outerchr13:101604033..101795231hg19UCSC Ensembl
Outerchr13:100402034..100593232hg18UCSC Ensembl
Outerchr13:100402034..100593232hg17UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38191102
hg19191199
hg18191199
hg17191199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1450452, nssv1450450
Samples
Known GenesNALCN, NALCN-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)nsv832699
Frequency
Sample Size95
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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