A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246886



Internal ID20813927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46244985..46245508hg38UCSC Ensembl
chr18:43824951..43825474hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576725
Supporting Variants
Samples
Known GenesC18orf25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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