A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878938



Internal ID22653905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67808174..67810118hg38UCSC Ensembl
chr16:67842077..67844021hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381945
hg191945
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479054
Samples
Known GenesTSNAXIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878938
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