A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887112



Internal ID22662104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12607477..12621292hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3813816
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1357n209
Supporting Variantsnssv17489386, nssv17489387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887112
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