A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105787



Internal ID22015020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41472581..41472581hg38UCSC Ensembl
chr21:42844508..42844508hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641196
Samples
Known GenesTMPRSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105787
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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