A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181787



Internal ID20748827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73432957..73441302hg38UCSC Ensembl
chr14:73899665..73908010hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg388346
hg198346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494982
Supporting Variants
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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