A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532638



Internal ID308556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45519072..45530419hg38UCSC Ensembl
chr20:44147712..44159058hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3811348
hg1911347
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532638
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