A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881521



Internal ID22656497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41492587..41494636hg38UCSC Ensembl
chr21:42864514..42866563hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382050
hg192050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488888
Samples
Known GenesTMPRSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881521
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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