A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102021



Internal ID22011254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59822228..59822228hg38UCSC Ensembl
chr20:58397283..58397283hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631478
Samples
Known GenesPHACTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102021
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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