A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669489



Internal ID21617795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37484416..37484416hg38UCSC Ensembl
chr22:37880454..37880454hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132153
SamplesHG03732
Known GenesMFNG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669489
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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