A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466768



Internal ID244599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173690183..173690240hg38UCSC Ensembl
chr5:173117186..173117243hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466768
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer