A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832863



Internal ID9423714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:94348482..94501487hg38UCSC Ensembl
Outerchr14:94814819..94967824hg19UCSC Ensembl
Outerchr14:93884572..94037577hg18UCSC Ensembl
Outerchr14:93884572..94037577hg17UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38153006
hg19153006
hg18153006
hg17153006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1451136
Samples
Known GenesSERPINA1, SERPINA11, SERPINA12, SERPINA9
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)nsv832863
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer