A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448664



Internal ID226931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115599433..115599495hg38UCSC Ensembl
chr3:115318280..115318342hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448664
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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