A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278907



Internal ID20845947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85271986..85272485hg38UCSC Ensembl
chr8:86184215..86184714hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568663
Supporting Variants
Samples
Known GenesCA13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278907
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00039


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