A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669869



Internal ID21618174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28471894..28637650hg38UCSC Ensembl
chr16:28483215..28648971hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38165757
hg19165757
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092278
SamplesHG00512
Known GenesAPOBR, CCDC101, CLN3, IL27, NUPR1, SULT1A1, SULT1A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669869
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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