A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245409



Internal ID20812449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59952759..59953443hg38UCSC Ensembl
chr18:57619991..57620675hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38685
hg19685
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245409
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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