A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086927



Internal ID21996160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39165443..39165443hg38UCSC Ensembl
chr11:39186993..39186993hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086927
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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