A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615691



Internal ID21563996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170241770..170241770hg38UCSC Ensembl
chr3:169959558..169959558hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136828
SamplesNA19239
Known GenesPRKCI
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615691
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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