A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671302



Internal ID21619607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41409666..41425380hg38UCSC Ensembl
chr21:42781593..42797307hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3815715
hg1915715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119330
Samples
Known GenesMX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671302
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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