A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085095



Internal ID21994328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58537288..58537288hg38UCSC Ensembl
chr16:58571192..58571192hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628789
Samples
Known GenesCNOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085095
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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