A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252119



Internal ID20819159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45004807..45005627hg38UCSC Ensembl
chr20:43633448..43634268hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597838
Supporting Variants
Samples
Known GenesSTK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252119
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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