A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478769



Internal ID21136322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65537605..65538811hg38UCSC Ensembl
chr14:66004323..66005529hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020748
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478769
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