A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466845



Internal ID244674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28746675..28763850hg38UCSC Ensembl
chr5:28746782..28763957hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3817176
hg1917176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466845
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