A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110515



Internal ID21293781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68288629..68294374hg38UCSC Ensembl
Innerchr17:66284770..66290515hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg385746
hg195746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv506n145
Supporting Variantsnssv14098628, nssv14097815
Samplessample378, sample296
Known GenesARSG, SLC16A6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110515
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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