A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521494



Internal ID297788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87268794..87269464hg38UCSC Ensembl
chr16:87302400..87303070hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521494
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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