A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072705



Internal ID21439519
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 StatusS
Merged Variantsnsv5657822
Supporting Variants
SamplesHG00732
Known GenesPPP2R1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072705
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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