A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113843



Internal ID21297109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:66560582..66577100hg38UCSC Ensembl
Innerchr16:66594485..66611003hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3816519
hg1916519
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097885
Samplessample396
Known GenesCKLF, CKLF-CMTM1, CMTM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113843
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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