A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117564



Internal ID21300830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39538298..39540696hg38UCSC Ensembl
Innerchr19:40028938..40031336hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382399
hg192399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv569n145
Supporting Variantsnssv14100442
Samplessample182
Known GenesEID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117564
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