A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027821



Internal ID21937164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38916310..39050351hg38UCSC Ensembl
chr11:38937860..39071901hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38134042
hg19134042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027821
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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