A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531479



Internal ID307439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68457256..68458088hg38UCSC Ensembl
chr16:68491159..68491991hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531479
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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