A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv160n97



Internal ID22815557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50055302..50135241hg38UCSC Ensembl
chr19:50558559..50638498hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3879940
hg1979940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155601, nsv1155602
Samples
Known GenesFLJ26850, SNAR-A10, SNAR-A11, SNAR-A14, SNAR-A3, SNAR-A4, SNAR-A5, SNAR-A6, SNAR-A7, SNAR-A8, SNAR-A9, SNAR-B1, SNAR-B2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv160n97
Frequency
Sample Size131
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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