A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873379



Internal ID22648325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31538494..31539793hg38UCSC Ensembl
chr22:31934480..31935779hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482865
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873379
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