A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099080



Internal ID21268225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:946625..971986hg38UCSC Ensembl
Innerchr16:996625..1021986hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3825362
hg1925362
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111946
Supporting Variants
Samplessample122
Known GenesLMF1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099080
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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