A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522837



Internal ID299095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56476685..56476834hg38UCSC Ensembl
chr16:56510597..56510746hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706018
Samples
Known GenesOGFOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522837
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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