A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235784



Internal ID20802824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118779804..118780618hg38UCSC Ensembl
chr11:118650513..118651327hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584967
Supporting Variants
Samples
Known GenesDDX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235784
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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