A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884496



Internal ID22659479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:15933654..15940385hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386732
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1358n209
Supporting Variantsnssv17489397, nssv17481412, nssv17489398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884496
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