A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663210



Internal ID21611515
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 StatusM
Merged Variants
Supporting Variantsnssv17092195, nssv17080838
SamplesHG00731, HG02011
Known GenesMRPL28
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663210
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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