A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957046



Internal ID38675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152180247..152182628hg38UCSC Ensembl
chr4:153101399..153103780hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382382
hg192382
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463296
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957046
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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