A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905273



Internal ID22680458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6490399..6496471hg38UCSC Ensembl
chr4:6492126..6498198hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386073
hg196073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425429
Samples
Known GenesPPP2R2C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905273
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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