A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874397



Internal ID22649349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13013895..13024361hg38UCSC Ensembl
chr16:13107752..13118218hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3810467
hg1910467
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475738
Samples
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874397
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