A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361973



Internal ID21019526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43285201..43287400hg38UCSC Ensembl
chr3:43326693..43328892hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208670
Samples
Known GenesSNRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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