A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481294



Internal ID21138847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60110828..60111363hg38UCSC Ensembl
chr14:60577546..60578081hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020474
Samples
Known GenesPCNXL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481294
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