A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521405



Internal ID297701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38870492..38871358hg38UCSC Ensembl
chr20:37499135..37500001hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732333
Samples
Known GenesPPP1R16B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521405
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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