A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277255



Internal ID20844295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140401633..140402269hg38UCSC Ensembl
chr8:141411732..141412368hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568817
Supporting Variants
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277255
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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