A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649658



Internal ID21597963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55518237..55518237hg38UCSC Ensembl
chr16:55552149..55552149hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg386087
hg196087
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083709
SamplesNA19239
Known GenesLPCAT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649658
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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