A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834568



Internal ID16111751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:231625367..231780141hg38UCSC Ensembl
Outerchr2:232490078..232644851hg19UCSC Ensembl
Outerchr2:232198322..232353095hg18UCSC Ensembl
Outerchr2:232315583..232470356hg17UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38154775
hg19154774
hg18154774
hg17154774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1442614
Samples
Known GenesMIR1244-1, MIR1244-2, MIR1244-3, PDE6D, PTMA
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)nsv834568
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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