A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv68n97



Internal ID22815465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31957801..31965910hg38UCSC Ensembl
chr13:32531938..32540047hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg388110
hg198110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154889, nsv1154888
Samples
Known GenesEEF1DP3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv68n97
Frequency
Sample Size131
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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