A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278064



Internal ID20845104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42859450..42859716hg38UCSC Ensembl
chr8:42714593..42714859hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559541
Supporting Variants
Samples
Known GenesRNF170
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278064
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