A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080838



Internal ID21436972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:370390..370390hg38UCSC Ensembl
chr16:420390..420390hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663210
Supporting Variants
SamplesHG00731
Known GenesMRPL28
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080838
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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