A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111232



Internal ID22020465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18708207..18708207hg38UCSC Ensembl
chr20:18688851..18688851hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632634
Samples
Known GenesDTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111232
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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