A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv65n97



Internal ID22815462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114967297..114980678hg38UCSC Ensembl
chr12:115405102..115418483hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3813382
hg1913382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154859, nsv1154858
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv65n97
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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