A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276130



Internal ID20843170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123519366..123519961hg38UCSC Ensembl
chr8:124531606..124532201hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567805
Supporting Variants
Samples
Known GenesFBXO32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276130
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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