A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116666



Internal ID21299932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65304876..65323087hg38UCSC Ensembl
Innerchr15:65597214..65615425hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3818212
hg1918212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095295
Samplessample14
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116666
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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