A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093859



Internal ID21286342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:1656970..1675728hg38UCSC Ensembl
Innerchr12:1766136..1784894hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3818759
hg1918759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111789
Supporting Variants
Samplessample386
Known GenesMIR3649
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093859
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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