A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111493



Internal ID21294759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39538921..39542152hg38UCSC Ensembl
Innerchr19:40029561..40032792hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383232
hg193232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101495
Samplessample361
Known GenesEID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111493
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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