A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117096



Internal ID21300362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39538921..39540804hg38UCSC Ensembl
Innerchr19:40029561..40031444hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381884
hg191884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv569n145
Supporting Variantsnssv14101310, nssv14101236
Samplessample289, sample86
Known GenesEID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117096
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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