A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093616



Internal ID22002849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64843580..64843580hg38UCSC Ensembl
chr15:65135779..65135779hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608269
Samples
Known GenesPLEKHO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093616
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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