A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272837



Internal ID20839877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99493205..99494656hg38UCSC Ensembl
chr6:99941081..99942532hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381452
hg191452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573919
Supporting Variants
Samples
Known GenesUSP45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272837
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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