A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654456



Internal ID21602761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111766393..111766393hg38UCSC Ensembl
chr11:111637117..111637117hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072706
SamplesNA19238
Known GenesPPP2R1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654456
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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