A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117666



Internal ID21300932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:106138051..106143282hg38UCSC Ensembl
Innerchr7:105778497..105783728hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg385232
hg195232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084889
Samplessample379
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117666
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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