A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100441



Internal ID21272764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33374309..33375328hg38UCSC Ensembl
Innerchr19:33865215..33866234hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381020
hg191020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113126
Supporting Variants
Samplessample182
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100441
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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