A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251707



Internal ID20818748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30942492..30996452hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3853961
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599309
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00424


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