A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662382



Internal ID21610687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89167122..89167122hg38UCSC Ensembl
chr12:89560899..89560899hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086815
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662382
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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