A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111961



Internal ID21295227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36987297..36992522hg38UCSC Ensembl
Innerchr8:36844815..36850040hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385226
hg195226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1170n145
Supporting Variantsnssv14087316
Samplessample300
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111961
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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