A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494013



Internal ID21151566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53846700..53854998hg38UCSC Ensembl
chr14:54313418..54321716hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg388299
hg198299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494013
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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