A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093269



Internal ID22002502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34093854..34093854hg38UCSC Ensembl
chr11:34115401..34115401hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595863
Samples
Known GenesCAPRIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093269
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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