A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274738



Internal ID20483956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147050920..147051019hg38UCSC Ensembl
chr5:146430483..146430582hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734482
Supporting Variants
Samples
Known GenesPPP2R2B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274738
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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