A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532720



Internal ID308633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59802859..59814185hg38UCSC Ensembl
chr16:59836763..59848089hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3811327
hg1911327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532720
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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