A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110883



Internal ID21294149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18024164..18031253hg38UCSC Ensembl
Innerchr19:18134973..18142063hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg387090
hg197091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100420
Samplessample176
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110883
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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