A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886406



Internal ID22661393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23643279..23644778hg38UCSC Ensembl
chr16:23654600..23656099hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477673
Samples
Known GenesDCTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886406
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