A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023807



Internal ID83585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83846552..83978552hg38UCSC Ensembl
chr9:86461467..86593467hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38132001
hg19132001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483168
Supporting Variants
Samples
Known GenesC9orf64, HNRNPK, KIF27, MIR7-1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023807
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000469


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