A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363878



Internal ID21021431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43015890..43016754hg38UCSC Ensembl
chr3:43057382..43058246hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208665
Samples
Known GenesFAM198A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363878
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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