A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419862



Internal ID198983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9533143..9606143hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3873001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419862
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