A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084502



Internal ID21993735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68998242..68998242hg38UCSC Ensembl
chr11:68765710..68765710hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084502
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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