A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245529



Internal ID20812569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67163472..67164171hg38UCSC Ensembl
chr18:64830709..64831408hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245529
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00028


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