A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466919



Internal ID244746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25335947..25388999hg38UCSC Ensembl
chr5:25336056..25389108hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3853053
hg1953053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16965229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466919
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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