A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv829812



Internal ID16106995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184136655..184302302hg38UCSC Ensembl
Outerchr3:183854443..184020090hg19UCSC Ensembl
Outerchr3:185337137..185502784hg18UCSC Ensembl
Outerchr3:185337145..185502792hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38165648
hg19165648
hg18165648
hg17165648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1443280, nssv1443279, nssv1443281
Samples
Known GenesABCF3, ALG3, AP2M1, CAMK2N2, DVL3, ECE2, EIF2B5, MIR1224, PSMD2, VWA5B2
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)nsv829812
Frequency
Sample Size95
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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