A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531784



Internal ID20905145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46755301..46758100hg38UCSC Ensembl
chr19:47258558..47261357hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198920
Samples
Known GenesFKRP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531784
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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