A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483326



Internal ID21140879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32200201..32206100hg38UCSC Ensembl
chr14:32669407..32675306hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483326
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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