A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180164



Internal ID20747204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93849366..93867308hg38UCSC Ensembl
chr14:94315712..94333654hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3817943
hg1917943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505783
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180164
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00046


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