A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518593



Internal ID20891954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39022923..39037971hg38UCSC Ensembl
chr19:39513563..39528611hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3815049
hg1915049
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198117
Samples
Known GenesFBXO27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518593
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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