A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16925903



Internal ID18022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216550097..216552712hg38UCSC Ensembl
chr2:217414820..217417435hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg382616
hg192616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16925903
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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