A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515854



Internal ID292328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59601502..59601568hg38UCSC Ensembl
chr20:58176557..58176623hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733384
Samples
Known GenesPHACTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515854
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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