A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111212



Internal ID21294478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:30221237..30229287hg38UCSC Ensembl
Innerchr19:30712144..30720194hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg388051
hg198051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv562n145
Supporting Variantsnssv14101486
Samplessample360
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111212
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