A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492463



Internal ID21150016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72815980..73092199hg38UCSC Ensembl
chr14:73282688..73558907hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38276220
hg19276220
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2194n223
Supporting Variantsnssv18178646
Samples
Known GenesDCAF4, DPF3, RBM25, ZFYVE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492463
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