A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733759



Internal ID157425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5142290..5142311hg38UCSC Ensembl
chr21:45539625..45539646hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539323
Supporting Variants
Samples
Known GenesPWP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733759
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00282


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