A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452818



Internal ID230961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37089131..37161322hg38UCSC Ensembl
chr3:37130622..37202813hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3872192
hg1972192
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932599
Samples
Known GenesLRRFIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452818
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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