A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559008



Internal ID332056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75981301..75981403hg38UCSC Ensembl
chr18:73693256..73693358hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719565
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559008
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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