A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757328



Internal ID20533188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111766408..111766408hg38UCSC Ensembl
chr11:111637132..111637132hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265123
Samples
Known GenesPPP2R1B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757328
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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