A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477330



Internal ID21134883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20701131..20706545hg38UCSC Ensembl
chr14:21169290..21174704hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg385415
hg195415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477330
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer