A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486461



Internal ID21144014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78499265..78562637hg38UCSC Ensembl
chr14:78965608..79028980hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3863373
hg1963373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020906
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486461
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