A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466239



Internal ID244084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108420614..108441602hg38UCSC Ensembl
chr5:107756315..107777303hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3820989
hg1920989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16973570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466239
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