A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253627



Internal ID20820667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1868345..1869387hg38UCSC Ensembl
chr20:1848991..1850033hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381043
hg191043
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596775
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253627
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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