A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463544



Internal ID241445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3312347..3312796hg38UCSC Ensembl
chr5:3312461..3312910hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463544
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