A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105936



Internal ID22015169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8643761..8643761hg38UCSC Ensembl
chr20:8624408..8624408hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623124
Samples
Known GenesPLCB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105936
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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