A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650238



Internal ID21598543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66874648..66874648hg38UCSC Ensembl
chr16:66908551..66908551hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091505
SamplesHG00733
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650238
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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