A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528141



Internal ID20901502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45696663..45713381hg38UCSC Ensembl
chr19:46199921..46216639hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3816719
hg1916719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198897
Samples
Known GenesFBXO46, QPCTL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528141
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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