A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419189



Internal ID198329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11683288..11701288hg38UCSC Ensembl
chr21:9680584..9698564hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3818001
hg1917981
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419189
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer