A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832890



Internal ID16110073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105304955..105483089hg38UCSC Ensembl
Outerchr14:105771292..105949426hg19UCSC Ensembl
Outerchr14:104842337..105020471hg18UCSC Ensembl
Outerchr14:104842337..105020471hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38178135
hg19178135
hg18178135
hg17178135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1451179, nssv1451176, nssv1451177, nssv1451181, nssv1451178, nssv1451180
Samples
Known GenesBRF1, CRIP2, MTA1, PACS2, TEX22
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)nsv832890
Frequency
Sample Size95
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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