A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497402



Internal ID20870608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89233820..89243765hg38UCSC Ensembl
chr14:89700164..89710109hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg389946
hg199946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022660
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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