A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516619



Internal ID293070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52259653..52260488hg38UCSC Ensembl
chr16:52293565..52294400hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516619
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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