A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526302



Internal ID302436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26785123..26785570hg38UCSC Ensembl
chr16:26796444..26796891hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526302
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