A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111234



Internal ID21294500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40511754..40515706hg38UCSC Ensembl
Innerchr19:41017661..41021613hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383953
hg193953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099688
Samplessample141
Known GenesSPTBN4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111234
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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