A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528085



Internal ID304156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52587449..52588566hg38UCSC Ensembl
chr16:52621361..52622478hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg381118
hg191118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707449
Samples
Known GenesCASC16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528085
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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