A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484769



Internal ID21142322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39418701..39445400hg38UCSC Ensembl
chr14:39887905..39914604hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3826700
hg1926700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187217
Samples
Known GenesFBXO33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484769
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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