A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869434



Internal ID22644369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42797352..42798451hg38UCSC Ensembl
chr22:43193358..43194457hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483612
Samples
Known GenesARFGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869434
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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