A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253481



Internal ID20820521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12748945..12854061hg38UCSC Ensembl
chr20:12729592..12834709hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38105117
hg19105118
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597383
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253481
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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