A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487583



Internal ID21145136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49524705..49525476hg38UCSC Ensembl
chr14:49991423..49992194hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487583
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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