A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455095



Internal ID233181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146609659..146615659hg38UCSC Ensembl
chr5:145989222..145995222hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974671
Samples
Known GenesPPP2R2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455095
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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