A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651799



Internal ID21600104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85643354..85643354hg38UCSC Ensembl
chr14:86109698..86109698hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090895
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651799
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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