A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089649



Internal ID21276764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:171149871..171152595hg38UCSC Ensembl
Innerchr1:171119010..171121734hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg382725
hg192725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112399
Supporting Variants
Samplessample241
Known GenesFMO6P
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089649
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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