A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523993



Internal ID300206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3634428..3643938hg38UCSC Ensembl
chr16:3684429..3693939hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389511
hg199511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523993
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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