A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650659



Internal ID21598964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92705312..92705312hg38UCSC Ensembl
chr11:92438478..92438478hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076418
SamplesHG03486
Known GenesFAT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650659
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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