A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278479



Internal ID20845519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66130695..66132460hg38UCSC Ensembl
chr8:67042930..67044695hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg381766
hg191766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574780
Supporting Variants
Samples
Known GenesTRIM55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278479
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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