A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517386



Internal ID293811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65369092..65393898hg38UCSC Ensembl
chr16:65402995..65427801hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3824807
hg1924807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710138
Samples
Known GenesLINC00922
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517386
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