A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113487



Internal ID21296753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18886183..18890967hg38UCSC Ensembl
Innerchr17:18789496..18794280hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg384785
hg194785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv481n145
Supporting Variantsnssv14098898
Samplessample146
Known GenesPRPSAP2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113487
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