A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278487



Internal ID20845527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66503152..66503854hg38UCSC Ensembl
chr8:67415387..67416089hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575222
Supporting Variants
Samples
Known GenesC8orf46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278487
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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