A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661349



Internal ID21609654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53906120..53906120hg38UCSC Ensembl
chr19:54409374..54409374hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106071
SamplesNA19650
Known GenesPRKCG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661349
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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