A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094178



Internal ID22003411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115776593..115776593hg38UCSC Ensembl
chr10:117536104..117536104hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584545
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094178
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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