A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434955



Internal ID213615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60714000..60778000hg38UCSC Ensembl
chr3:60699733..60763733hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3864001
hg1964001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932922
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434955
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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