A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1445890



Internal ID16096494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:5208526..5387834hg38UCSC Ensembl
Outerchr7:5248157..5427465hg19UCSC Ensembl
Outerchr7:5214683..5393991hg18UCSC Ensembl
Outerchr7:5021398..5200706hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38179309
hg19179309
hg18179309
hg17179309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv830889
Supporting Variants
Samples
Known GenesSLC29A4, TNRC18, WIPI2
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)nssv1445890
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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