A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089897



Internal ID21999130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111766411..111766411hg38UCSC Ensembl
chr11:111637135..111637135hg19UCSC 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 Variantsnssv17610825
Samples
Known GenesPPP2R1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089897
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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