A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524688



Internal ID300884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77339123..77339894hg38UCSC Ensembl
chr16:77373020..77373791hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709744
Samples
Known GenesADAMTS18
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524688
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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