A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727037



Internal ID150703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42058781..42060204hg38UCSC Ensembl
chr21:43478890..43480313hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381424
hg191424
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727037
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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