A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269166



Internal ID20478384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129889661..129889661hg38UCSC Ensembl
chr11:129759556..129759556hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761431
Supporting Variants
Samples
Known GenesNFRKB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269166
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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