A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878170



Internal ID22653134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18048579..18049978hg38UCSC Ensembl
chr22:18531345..18532744hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878170
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