A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240811



Internal ID20807851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74686124..74686466hg38UCSC Ensembl
chr16:74720022..74720364hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584541
Supporting Variants
Samples
Known GenesMLKL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240811
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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