A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1452799



Internal ID16103403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:61558794..61736777hg38UCSC Ensembl
Outerchr16:61592698..61770681hg19UCSC Ensembl
Outerchr16:60150199..60328182hg18UCSC Ensembl
Outerchr16:60150199..60328182hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38177984
hg19177984
hg18177984
hg17177984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv833256
Supporting Variants
Samples
Known GenesCDH8
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)nssv1452799
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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