A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252076



Internal ID20819116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43632270..43633241hg38UCSC Ensembl
chr20:42260910..42261881hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595788
Supporting Variants
Samples
Known GenesIFT52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00037


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