A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478589



Internal ID21136142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54921286..54934238hg38UCSC Ensembl
chr14:55388004..55400956hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3812953
hg1912953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478589
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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