A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940419



Internal ID27662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143599607..143616466hg38UCSC Ensembl
chr3:143318449..143335308hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3816860
hg1916860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435196
Supporting Variants
Samples
Known GenesSLC9A9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940419
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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