A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481939



Internal ID21139492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54015194..54023284hg38UCSC Ensembl
chr14:54481912..54490002hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg388091
hg198091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481939
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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