A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561254



Internal ID334239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3982064..3982510hg38UCSC Ensembl
chr20:3962711..3963157hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730473
Samples
Known GenesRNF24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561254
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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