A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592787



Internal ID21541371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39277672..39277759hg38UCSC Ensembl
chr14:39746876..39746963hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082002
SamplesHG00732
Known GenesCTAGE5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592787
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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