A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464053



Internal ID241939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64066484..64093489hg38UCSC Ensembl
chr5:63362311..63389316hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3827006
hg1927006
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16966648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464053
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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