A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243992



Internal ID20811032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:29065280..29066677hg38UCSC Ensembl
chr18:26645244..26646641hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381398
hg191398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243992
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