A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278497



Internal ID20845537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66668503..66669368hg38UCSC Ensembl
chr8:67580738..67581603hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562237
Supporting Variants
Samples
Known GenesC8orf44, C8orf44-SGK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278497
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