A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254109



Internal ID20821149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6878881..6879387hg38UCSC Ensembl
chr20:6859528..6860034hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254109
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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