A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104466



Internal ID22013699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22949906..22949906hg38UCSC Ensembl
chr20:22930543..22930543hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104466
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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