A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459388



Internal ID237403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45955610..45955721hg38UCSC Ensembl
chr4:45957627..45957738hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16949899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459388
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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