A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655012



Internal ID21603317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76376748..76376748hg38UCSC Ensembl
chr11:76087792..76087792hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076159
SamplesHG03125
Known GenesPRKRIR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655012
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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