A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110790



Internal ID21294056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119077339..119080240hg38UCSC Ensembl
Innerchr6:119398504..119401405hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382902
hg192902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1065n145
Supporting Variantsnssv14086410
Samplessample139
Known GenesFAM184A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110790
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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