A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246119



Internal ID20813159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:222583..223106hg38UCSC Ensembl
chr18:222583..223106hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576308
Supporting Variants
Samples
Known GenesTHOC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246119
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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