A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592178



Internal ID21540759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22436053..22436739hg38UCSC Ensembl
chr16:22447374..22448060hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090311
SamplesNA19238
Known GenesRRN3P3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592178
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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