A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278808



Internal ID20845848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80455907..80456296hg38UCSC Ensembl
chr8:81368142..81368531hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278808
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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