A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524289



Internal ID20897650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38949480..38984502hg38UCSC Ensembl
chr19:39440120..39475142hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3835023
hg1935023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198115
Samples
Known GenesFBXO17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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