A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555041



Internal ID328209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19276739..19277244hg38UCSC Ensembl
chr21:20649056..20649561hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555041
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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