A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116870



Internal ID21300136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26855236..26863656hg38UCSC Ensembl
Innerchr4:26856858..26865278hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg388421
hg198421
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv869n145
Supporting Variantsnssv14096591
Samplessample412
Known GenesSTIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116870
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