A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932599



Internal ID22444
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 StatusS
Merged Variantsnsv5452818
Supporting Variants
Samples
Known GenesLRRFIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932599
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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