A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910796



Internal ID7964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15963818..15963887hg38UCSC Ensembl
chr2:16103940..16104009hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448518
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910796
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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