A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956241



Internal ID38132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:116743745..116777402hg38UCSC Ensembl
chr4:117664901..117698558hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3833658
hg1933658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956241
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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