A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479923



Internal ID21137476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32478610..32492095hg38UCSC Ensembl
chr14:32947816..32961301hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3813486
hg1913486
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189003
Samples
Known GenesAKAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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