A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111857



Internal ID21295123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33373420..33374983hg38UCSC Ensembl
Innerchr19:33864326..33865889hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381564
hg191564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100548, nssv14101928
Samplessample111, sample227
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111857
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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