A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252128



Internal ID20819168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:455681..456826hg38UCSC Ensembl
chr20:436325..437470hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596432
Supporting Variants
Samples
Known GenesTBC1D20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252128
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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