A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533863



Internal ID309741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53714813..53732557hg38UCSC Ensembl
chr16:53748725..53766469hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3817745
hg1917745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705916
Samples
Known GenesFTO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533863
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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