A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453786



Internal ID231898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60999004..61077774hg38UCSC Ensembl
chr3:60984676..61063447hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3878771
hg1978772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934667
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453786
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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