A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478902



Internal ID21136455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41983164..42077680hg38UCSC Ensembl
chr14:42452367..42546883hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3894517
hg1994517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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