A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523067



Internal ID299316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62808474..62815963hg38UCSC Ensembl
chr16:62842378..62849867hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387490
hg197490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523067
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer