A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652027



Internal ID21600332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58507253..58507253hg38UCSC Ensembl
chr14:58973971..58973971hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092319
SamplesHG03065
Known GenesKIAA0586
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652027
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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