A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106712



Internal ID22015946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23009063..23009063hg38UCSC Ensembl
chr20:22989700..22989700hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106712
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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