A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832417



Internal ID16109600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:53075874..53254231hg38UCSC Ensembl
Outerchr12:53469658..53648015hg19UCSC Ensembl
Outerchr12:51755925..51934282hg18UCSC Ensembl
Outerchr12:51755925..51934282hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38178358
hg19178358
hg18178358
hg17178358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1449843
Samples
Known GenesCSAD, IGFBP6, ITGB7, MFSD5, RARG, SOAT2, SPRYD3, ZNF740
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)nsv832417
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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