A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535200



Internal ID20908561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45721242..45722992hg38UCSC Ensembl
chr19:46224500..46226250hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381751
hg191751
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198899
Samples
Known GenesFBXO46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535200
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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