A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666308



Internal ID21614613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35718782..35718782hg38UCSC Ensembl
chr22:36114829..36114829hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3821283
hg1921283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137129
SamplesHG02587
Known GenesAPOL5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666308
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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