A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483738



Internal ID21141291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84171740..84172367hg38UCSC Ensembl
chr14:84638084..84638711hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483738
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