A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv32n68



Internal ID20147801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:245507..476226hg38UCSC Ensembl
chr16:295506..526226hg19UCSC Ensembl
chr16:235507..466227hg18UCSC Ensembl
chr16:235507..466227hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38230720
hg19230721
hg18230721
hg17230721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv833111, nsv833112
Samples
Known GenesARHGDIG, AXIN1, DECR2, ITFG3, LOC100134368, MRPL28, NME4, PDIA2, RAB11FIP3, RGS11, TMEM8A
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)dgv32n68
Frequency
Sample Size95
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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