A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523653



Internal ID299878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28157175..28157260hg38UCSC Ensembl
chr16:28168496..28168581hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706310
Samples
Known GenesXPO6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523653
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