A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727402



Internal ID151068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11683288..11701288hg38UCSC Ensembl
chr21:9680584..9698564hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3818001
hg1917981
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727402
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.474335


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