A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106171



Internal ID22015404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34258815..34258815hg38UCSC Ensembl
chr20:32846621..32846621hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106171
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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