A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16921726



Internal ID15257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161010706..161029483hg38UCSC Ensembl
chr2:161867217..161885994hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3818778
hg1918778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16921726
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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