A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366882



Internal ID21024435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65587446..65597793hg38UCSC Ensembl
chr3:65573121..65583468hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3810348
hg1910348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212976
Samples
Known GenesMAGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366882
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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