A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110771



Internal ID21294037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:13827082..13831362hg38UCSC Ensembl
Innerchr18:13827081..13831361hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg384281
hg194281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100229
Samplessample329
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110771
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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