A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111717



Internal ID21294983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89830771..89842124hg38UCSC Ensembl
Innerchr3:89879921..89891274hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3811354
hg1911354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105288
Samplessample96
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111717
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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