A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106036



Internal ID22015269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32954827..32954827hg38UCSC Ensembl
chr19:33445733..33445733hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636517
Samples
Known GenesCEP89
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106036
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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