A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185002



Internal ID20752042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89381352..89395931hg38UCSC Ensembl
chr14:89847696..89862275hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3814580
hg1914580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497307
Supporting Variants
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185002
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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