A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864015



Internal ID22638950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89909971..89912271hg38UCSC Ensembl
chr14:90376315..90378615hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470348
Samples
Known GenesEFCAB11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864015
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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