A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117078



Internal ID21300344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65053404..65058829hg38UCSC Ensembl
Innerchr17:63049522..63054947hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg385426
hg195426
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098668
Samplessample397
Known GenesGNA13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117078
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