A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252579



Internal ID20819619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49779827..49780846hg38UCSC Ensembl
chr20:48396364..48397383hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg381020
hg191020
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598058
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00024


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