A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889926



Internal ID22664948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146846106..146846405hg38UCSC Ensembl
chr5:146225669..146225968hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426851
Samples
Known GenesPPP2R2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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