A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455604



Internal ID233682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44919361..44934479hg38UCSC Ensembl
chr5:44919463..44934581hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3815119
hg1915119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16965462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455604
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