A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244065



Internal ID20811105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32065530..32066172hg38UCSC Ensembl
chr18:29645493..29646135hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575898
Supporting Variants
Samples
Known GenesRNF125
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244065
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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