A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515388



Internal ID20888747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89199826..89272725hg38UCSC Ensembl
chr14:89666170..89739069hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3872900
hg1972900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021633
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515388
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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