A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663206



Internal ID21611511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60108768..60108768hg38UCSC Ensembl
chr14:60575486..60575486hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098016
SamplesHG00731
Known GenesPCNXL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663206
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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