A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872057



Internal ID22646995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25969799..25972027hg38UCSC Ensembl
chr22:26365765..26367993hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382229
hg192229
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482810
Samples
Known GenesMYO18B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872057
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