A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485871



Internal ID21143424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55222663..55271586hg38UCSC Ensembl
chr14:55689381..55738304hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3848924
hg1948924
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191659
Samples
Known GenesFBXO34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485871
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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