A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111215



Internal ID21294481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7716468..7724880hg38UCSC Ensembl
Innerchr19:7781354..7789766hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg388413
hg198413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099659
Samplessample134
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111215
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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