A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937316



Internal ID25600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95277645..95326442hg38UCSC Ensembl
chr3:94996489..95045286hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3848798
hg1948798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451031
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937316
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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