A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106040



Internal ID22015273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43777125..43777125hg38UCSC Ensembl
chr20:42405765..42405765hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg382258
hg192258
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106040
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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