A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115525



Internal ID21298791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160567721..160707545hg38UCSC Ensembl
Innerchr4:161488873..161628697hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38139825
hg19139825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093447
Samplessample291
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115525
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