A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv105n97



Internal ID22815502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15100205..15388077hg38UCSC Ensembl
chr16:15194062..15481934hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38287873
hg19287873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155245, nsv1155246
Samples
Known GenesMIR3180-4, MIR6511B-1, NPIPA5, PDXDC1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv105n97
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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