A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090392



Internal ID21999625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45827212..45827212hg38UCSC Ensembl
chr11:45848763..45848763hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090392
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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