A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516132



Internal ID292597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63107979..63189258hg38UCSC Ensembl
chr16:63141883..63223162hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3881280
hg1981280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516132
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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