A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143602



Internal ID342803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64251883..64251940hg38UCSC Ensembl
chr11:64019355..64019412hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046705
Samples
Known GenesPLCB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143602
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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