A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034796



Internal ID21944139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121185264..121185926hg38UCSC Ensembl
chr11:121055973..121056635hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617517
Samples
Known GenesTECTA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034796
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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