A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv829839



Internal ID16453708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:2622695..2657883hg38UCSC Ensembl
Outerchr4:2624422..2659610hg19UCSC Ensembl
Outerchr4:2594220..2629408hg18UCSC Ensembl
Outerchr4:2661628..2696816hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3835189
hg1935189
hg1835189
hg1735189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1443331
Samples
Known GenesFAM193A
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)nsv829839
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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