A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653921



Internal ID21602226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16559383..16559383hg38UCSC Ensembl
chr11:16580930..16580930hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073406
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653921
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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