A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520056



Internal ID296396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84569094..84602270hg38UCSC Ensembl
chr16:84602700..84635876hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3833177
hg1933177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708332
Samples
Known GenesCOTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520056
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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