A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099259



Internal ID22008492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57480226..57480226hg38UCSC Ensembl
chr15:57772424..57772424hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604973
Samples
Known GenesCGNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099259
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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