A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993881



Internal ID21903224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60672673..60817070hg38UCSC Ensembl
chr3:60658406..60802774hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38144398
hg19144369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551820
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993881
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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