A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662133



Internal ID21610438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46161920..46161920hg38UCSC Ensembl
chr11:46183471..46183471hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074730
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662133
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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