A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657822



Internal ID21606127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111746202..111746202hg38UCSC Ensembl
chr11:111616926..111616926hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072705
SamplesHG00732
Known GenesPPP2R1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657822
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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