A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651104



Internal ID21599409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105229625..105229625hg38UCSC Ensembl
chr14:105695962..105695962hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091562, nssv17097559
SamplesHG00096, HG03486
Known GenesBRF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651104
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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