A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111974



Internal ID21295240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110819377..110869369hg38UCSC Ensembl
Innerchr10:112579135..112629127hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3849993
hg1949993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090115
Samplessample119
Known GenesPDCD4-AS1, RBM20
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111974
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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