A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086812



Internal ID21284389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20776035..20788174hg38UCSC Ensembl
Innerchr7:20815655..20827793hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3812140
hg1912139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114668
Supporting Variants
Samplessample360
Known GenesSP8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086812
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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