A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429279



Internal ID208129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10924600..10966000hg38UCSC Ensembl
chrUn_gl000241:28..41428hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3841401
hg1941401
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429279
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