A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv829654



Internal ID16106837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:107435249..107587384hg38UCSC Ensembl
Outerchr3:107154096..107306231hg19UCSC Ensembl
Outerchr3:108636786..108788921hg18UCSC Ensembl
Outerchr3:108636786..108788921hg17UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38152136
hg19152136
hg18152136
hg17152136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1442965, nssv1442966
Samples
Known GenesBBX
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)nsv829654
Frequency
Sample Size95
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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