A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111705



Internal ID21294971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154886530..154894752hg38UCSC Ensembl
Innerchr3:154604319..154612541hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg388223
hg198223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108613
Samplessample367
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111705
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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