A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667689



Internal ID21615994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44827484..44875420hg38UCSC Ensembl
chr21:46247399..46295335hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3847937
hg1947937
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119460
Samples
Known GenesPTTG1IP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667689
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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