A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195478



Internal ID20762518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77401113..77405133hg38UCSC Ensembl
chr14:77867456..77871476hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384021
hg194021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476763
Supporting Variants
Samples
Known GenesNOXRED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195478
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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