A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253579



Internal ID20820619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16660646..16661112hg38UCSC Ensembl
chr20:16641291..16641757hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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