A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663123



Internal ID21611428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61821164..61821164hg38UCSC Ensembl
chr14:62287882..62287882hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091456
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663123
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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