A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051625



Internal ID21960858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8629873..8629952hg38UCSC Ensembl
chr20:8610520..8610599hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624644
Samples
Known GenesPLCB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051625
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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