A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661221



Internal ID21609526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11966402..11966402hg38UCSC Ensembl
chr16:12060259..12060259hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097216
SamplesHG02818
Known GenesTNFRSF17
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661221
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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