A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453179



Internal ID231312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192452235..192452306hg38UCSC Ensembl
chr3:192170024..192170095hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735029
Samples
Known GenesFGF12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453179
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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