A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098819



Internal ID22008052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27318670..27318670hg38UCSC Ensembl
chr16:27329991..27329991hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633502
Samples
Known GenesIL4R
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098819
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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