A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576266



Internal ID20949337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23467339..23468035hg38UCSC Ensembl
chr18:21047303..21047999hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246780
Samples
Known GenesRIOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576266
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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