A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832787



Internal ID16456656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:46310493..46466233hg38UCSC Ensembl
Outerchr14:46779696..46935436hg19UCSC Ensembl
Outerchr14:45849446..46005186hg18UCSC Ensembl
Outerchr14:45849446..46005186hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38155741
hg19155741
hg18155741
hg17155741
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1450949, nssv1450951
Samples
Known GenesLINC00871
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)nsv832787
Frequency
Sample Size95
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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