A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244792



Internal ID20811832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:72328273..72367402hg38UCSC Ensembl
chr18:69995508..70034637hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3839130
hg1939130
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599893
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244792
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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