A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484567



Internal ID21142120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49216210..49216642hg38UCSC Ensembl
chr14:49682928..49683360hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484567
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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