A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1451004



Internal ID16101608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:65006526..65177927hg38UCSC Ensembl
Outerchr14:65473244..65644645hg19UCSC Ensembl
Outerchr14:64542997..64714398hg18UCSC Ensembl
Outerchr14:64542997..64714398hg17UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38171402
hg19171402
hg18171402
hg17171402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv832816
Supporting Variants
Samples
Known GenesCHURC1-FNTB, FNTB, LOC100506321, MAX, MIR4706
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)nssv1451004
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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