A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927834



Internal ID22703066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863246..106770580hg38UCSC Ensembl
chr14:106329456..107178822hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38907335
hg19849367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv647n209
Supporting Variantsnssv17383771
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927834
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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