A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649481



Internal ID21597786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70411162..70411162hg38UCSC Ensembl
chr11:70257268..70257268hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075517
SamplesNA19238
Known GenesCTTN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649481
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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