A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117926



Internal ID21301192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31197905..31214506hg38UCSC Ensembl
Innerchr19:31688811..31705412hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3816602
hg1916602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100414
Samplessample173
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117926
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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