A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652579



Internal ID21600884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51270634..51270634hg38UCSC Ensembl
chr16:51304545..51304545hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091771
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652579
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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