A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909882



Internal ID7358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6022203..6022334hg38UCSC Ensembl
chr2:6162335..6162466hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909882
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.047612


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