A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437422



Internal ID216012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73091489..73095969hg38UCSC Ensembl
chr3:73140640..73145120hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg384481
hg194481
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437422
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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