A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495254



Internal ID21152807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65711701..65721100hg38UCSC Ensembl
chr14:66178419..66187818hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195652
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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