A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv111n97



Internal ID22815508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22430699..22706267hg38UCSC Ensembl
chr16:22442020..22717588hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38275569
hg19275569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155287, nsv1155288
Samples
Known GenesLOC653786, NPIPB5, RRN3P3, SMG1P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv111n97
Frequency
Sample Size131
Observed Gain122
Observed Loss0
Observed Complex0
Frequencyn/a


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