A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859830



Internal ID22634765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67514007..67515006hg38UCSC Ensembl
chr14:67980724..67981723hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451421, nssv17458408
Samples
Known GenesTMEM229B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859830
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