A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511639



Internal ID20884969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89546892..89591866hg38UCSC Ensembl
chr14:90013236..90058210hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3844975
hg1944975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022672
Samples
Known GenesFOXN3, FOXN3-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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