A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470791



Internal ID248538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31555455..31558138hg38UCSC Ensembl
chr5:31555562..31558245hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg382684
hg192684
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470791
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