A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2116n209



Internal ID22828191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42728117..42731038hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382922
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5863414, nsv5851534, nsv5853580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2116n209
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