A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489355



Internal ID21146908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39472482..39513218hg38UCSC Ensembl
chr14:39941686..39982422hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3840737
hg1940737
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489355
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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