A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446536



Internal ID224859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59888376..60159063hg38UCSC Ensembl
chr3:59874102..60144791hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38270688
hg19270690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv346n206
Supporting Variantsnssv16932862
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446536
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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