A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463296



Internal ID241202
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 StatusM
Merged Variants
Supporting Variantsnssv16957046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463296
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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