A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663058



Internal ID21611363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23203459..23203459hg38UCSC Ensembl
chr14:23672668..23672668hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083913
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663058
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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