A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566100



Internal ID16006823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104863089..104865817hg38UCSC Ensembl
Innerchr14:105329426..105332154hg19UCSC Ensembl
Innerchr14:104400471..104403199hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg382729
hg192729
hg182729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3964n54
Supporting Variantsnssv834640
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566100
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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