A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097885



Internal ID21286970
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 StatusS
Merged Variantsnsv3113843
Supporting Variants
Samplessample396
Known GenesCKLF, CKLF-CMTM1, CMTM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097885
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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