A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927510



Internal ID19055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186907388..187063054hg38UCSC Ensembl
chr2:187772115..187927781hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38155667
hg19155667
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451169
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927510
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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