A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504321



Internal ID20877582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89354854..89359192hg38UCSC Ensembl
chr14:89821198..89825536hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg384339
hg194339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022663
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504321
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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