A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666325



Internal ID21614630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44088880..44088880hg38UCSC Ensembl
chr21:45508761..45508761hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381103
hg191103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119445
SamplesHG02011
Known GenesTRAPPC10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666325
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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