A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520563



Internal ID296888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38858156..38867553hg38UCSC Ensembl
chr20:37486799..37496196hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg389398
hg199398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732331
Samples
Known GenesPPP1R16B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520563
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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