A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450777



Internal ID228973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67155516..67279812hg38UCSC Ensembl
chr3:67205940..67330236hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38124297
hg19124297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934765
Samples
Known GenesMIR4272
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450777
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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