A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111135



Internal ID21294401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16470415..16471295hg38UCSC Ensembl
Innerchr19:16581226..16582106hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101465
Samplessample349
Known GenesEPS15L1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111135
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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