A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186838



Internal ID20753878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63677364..63678327hg38UCSC Ensembl
chr14:64144082..64145045hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485469
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186838
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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