A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659858



Internal ID21608163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58790184..58790184hg38UCSC Ensembl
chr14:59256902..59256902hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080606
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659858
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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