A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566108



Internal ID16006831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104863421..104866043hg38UCSC Ensembl
Innerchr14:105329758..105332380hg19UCSC Ensembl
Innerchr14:104400803..104403425hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg382623
hg192623
hg182623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3964n54
Supporting Variantsnssv834657, nssv834658, nssv834659
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566108
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer