A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100583



Internal ID22009816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32745965..32745965hg38UCSC Ensembl
chr20:31333771..31333771hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg382038
hg192038
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100583
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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