A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436152



Internal ID214774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65494826..65527430hg38UCSC Ensembl
chr3:65480501..65513105hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3832605
hg1932605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934987
Samples
Known GenesMAGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436152
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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