A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663365



Internal ID21611670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120389650..120389650hg38UCSC Ensembl
chr12:120827453..120827453hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17077470
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663365
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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