A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634716



Internal ID21583021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146716195..146716195hg38UCSC Ensembl
chr5:146095758..146095758hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123147
SamplesNA19238
Known GenesPPP2R2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634716
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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