A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459753



Internal ID237763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117832933..117883083hg38UCSC Ensembl
chr5:117168628..117218778hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3850151
hg1950151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv407n206
Supporting Variantsnssv16972807
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459753
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