A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946028



Internal ID31364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197005798..197005888hg38UCSC Ensembl
chr3:196732669..196732759hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439660
Supporting Variants
Samples
Known GenesMFI2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946028
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.256791


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