A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024741



Internal ID21934084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63418731..63435305hg38UCSC Ensembl
chr11:63186203..63202777hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3816575
hg1916575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592573
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024741
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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