A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834676



Internal ID16111859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:44928707..45149356hg38UCSC Ensembl
Outerchr3:44970199..45190848hg19UCSC Ensembl
Outerchr3:44945203..45165852hg18UCSC Ensembl
Outerchr3:44945203..45165852hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38220650
hg19220650
hg18220650
hg17220650
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1442771, nssv1442766, nssv1442756, nssv1442760, nssv1442770, nssv1442759, nssv1442765, nssv1442755, nssv1442769, nssv1442762, nssv1442764, nssv1442758, nssv1442768, nssv1442767, nssv1442757, nssv1442761
Samples
Known GenesCDCP1, CLEC3B, EXOSC7, ZDHHC3
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)nsv834676
Frequency
Sample Size95
Observed Gain7
Observed Loss9
Observed Complex0
Frequencyn/a


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