A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558852



Internal ID331905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55116667..55131397hg38UCSC Ensembl
chr20:53733206..53747936hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3814731
hg1914731
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558852
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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