A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097856



Internal ID21286072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35333706..35951191hg38UCSC Ensembl
Innerchr16:34568077..35185562hg19UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38617486
hg19617486
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111886
Supporting Variants
Samplessample382
Known GenesFLJ26245, LOC100130700, LOC146481, LOC283914
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097856
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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