A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666964



Internal ID21615269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43897530..43897530hg38UCSC Ensembl
chr21:45317411..45317411hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119437
SamplesHG00731
Known GenesAGPAT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666964
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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