A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976257



Internal ID51567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147001157..147012737hg38UCSC Ensembl
chr5:146380720..146392300hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3811581
hg1911581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461630
Supporting Variants
Samples
Known GenesPPP2R2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976257
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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