A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859466



Internal ID22634401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98475995..98478248hg38UCSC Ensembl
chr13:99128249..99130502hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg382254
hg192254
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv560n209
Supporting Variantsnssv17469622, nssv17461063
Samples
Known GenesSTK24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859466
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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