A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17539099



Internal ID21863454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73530716..73530849hg38UCSC Ensembl
chr3:73579867..73580000hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993953
Supporting Variants
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17539099
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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