A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459771



Internal ID237780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102135807..102189807hg38UCSC Ensembl
chr5:101471511..101525511hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3854001
hg1954001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16972536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459771
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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