A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734500



Internal ID158166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25579537..25579619hg38UCSC Ensembl
chr21:26951849..26951931hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515283
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734500
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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