A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460055



Internal ID238053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73974171..73974524hg38UCSC Ensembl
chr5:73269996..73270349hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16966801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460055
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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