A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524039



Internal ID300252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62489086..62500776hg38UCSC Ensembl
chr20:61064142..61075832hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3811691
hg1911691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733577
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524039
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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