A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096591



Internal ID21288124
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 StatusS
Merged Variantsnsv3116870
Supporting Variants
Samplessample412
Known GenesSTIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096591
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