A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518946



Internal ID295307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87538440..87539069hg38UCSC Ensembl
chr16:87572046..87572675hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518946
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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