A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544687



Internal ID21869042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73004910..73004970hg38UCSC Ensembl
chr3:73054061..73054121hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993950
Supporting Variants
Samples
Known GenesPPP4R2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544687
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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