A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278771



Internal ID20845811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79304035..79376919hg38UCSC Ensembl
chr8:80216270..80289154hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3872885
hg1972885
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278771
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00048


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