A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244047



Internal ID20811087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31940352..31940828hg38UCSC Ensembl
chr18:29520315..29520791hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580500
Supporting Variants
Samples
Known GenesTRAPPC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244047
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00042


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