A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566128



Internal ID16006851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104865139..104865880hg38UCSC Ensembl
Innerchr14:105331476..105332217hg19UCSC Ensembl
Innerchr14:104402521..104403262hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38742
hg19742
hg18742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3970n54
Supporting Variantsnssv834700
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566128
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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