A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254433



Internal ID20821473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9946298..9963067hg38UCSC Ensembl
chr20:9926946..9943715hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3816770
hg1916770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598553
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254433
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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