A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082792



Internal ID21992025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92154491..92154491hg38UCSC Ensembl
chr15:92697721..92697721hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606479
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082792
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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