A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035493



Internal ID21944836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58533664..58533961hg38UCSC Ensembl
chr16:58567568..58567865hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635300
Samples
Known GenesCNOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035493
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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