A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459559



Internal ID237571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82413423..82414995hg38UCSC Ensembl
chr4:83334576..83336148hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg381573
hg191573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459559
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