A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945017



Internal ID30676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6337122..6340040hg38UCSC Ensembl
chr4:6338849..6341767hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg382919
hg192919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447952
Supporting Variants
Samples
Known GenesPPP2R2C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945017
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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