A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867014



Internal ID22641949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105727796..105730881hg38UCSC Ensembl
chr9:108490077..108493162hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg383086
hg193086
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510601
Samples
Known GenesTMEM38B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867014
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