A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1443452



Internal ID16440742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:19266659..19431249hg38UCSC Ensembl
Outerchr4:19268282..19432872hg19UCSC Ensembl
Outerchr4:18877380..19041970hg18UCSC Ensembl
Outerchr4:18944551..19109141hg17UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38164591
hg19164591
hg18164591
hg17164591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv829872
Supporting Variants
Samples
Known Genes
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)nssv1443452
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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