A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663233



Internal ID21611538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123692219..123692219hg38UCSC Ensembl
chr11:123562927..123562927hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073059
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663233
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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