A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650132



Internal ID21598437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105231871..105231871hg38UCSC Ensembl
chr14:105698208..105698208hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087069
SamplesHG00732
Known GenesBRF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650132
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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