A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483972



Internal ID21141525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66003130..66498364hg38UCSC Ensembl
chr14:66469848..66965082hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38495235
hg19495235
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2179n223
Supporting Variantsnssv18183346
Samples
Known GenesLINC00238
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483972
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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