A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882913



Internal ID22657890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66968581..66969825hg38UCSC Ensembl
chr16:67002484..67003728hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472271, nssv17472272
Samples
Known GenesCES3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882913
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