A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660108



Internal ID21608413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64914235..64914235hg38UCSC Ensembl
chr12:65308015..65308015hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096643
SamplesHG03065
Known GenesFLJ41278
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660108
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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