A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494838



Internal ID21152391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41826201..42011400hg38UCSC Ensembl
chr14:42295404..42480603hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38185200
hg19185200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192261
Samples
Known GenesLRFN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494838
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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