A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832646



Internal ID16109829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:75726292..75908966hg38UCSC Ensembl
Outerchr13:76300428..76483102hg19UCSC Ensembl
Outerchr13:75198429..75381103hg18UCSC Ensembl
Outerchr13:75198429..75381103hg17UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38182675
hg19182675
hg18182675
hg17182675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1450358
Samples
Known GenesC13orf45, LMO7
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)nsv832646
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