A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089440



Internal ID21998673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65802211..65802211hg38UCSC Ensembl
chr15:66094549..66094549hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089440
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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