A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239984



Internal ID20807024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34588347..34956072hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38367726
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239984
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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