A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089429



Internal ID21998662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65965603..65965603hg38UCSC Ensembl
chr15:66257941..66257941hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600595
Samples
Known GenesMEGF11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089429
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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