A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193959



Internal ID20760999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65869000..66393077hg38UCSC Ensembl
chr14:66335718..66859795hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38524078
hg19524078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476783
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193959
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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