A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022118



Internal ID21931461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69813701..69813816hg38UCSC Ensembl
chr11:69628469..69628584hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595040
Samples
Known GenesFGF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022118
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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