A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485597



Internal ID21143150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79775648..79785032hg38UCSC Ensembl
chr14:80241991..80251375hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg389385
hg199385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179473
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485597
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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