A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479688



Internal ID21137241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84093901..84102600hg38UCSC Ensembl
chr14:84560245..84568944hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479688
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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