A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664466



Internal ID21612771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:282449..282449hg38UCSC Ensembl
chr19:282449..282449hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104327
SamplesHG03486
Known GenesPPAP2C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664466
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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