A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536469



Internal ID311945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57578465..57578465hg38UCSC Ensembl
chr3:57564192..57564192hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934851
Samples
Known GenesARF4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536469
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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