A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663936



Internal ID21612241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111639404..111639404hg38UCSC Ensembl
chr12:112077208..112077208hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17077189
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663936
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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