A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519281



Internal ID295633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86796071..86829559hg38UCSC Ensembl
chr16:86829677..86863165hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3833489
hg1933489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519281
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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