A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116390



Internal ID21299656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39478017..39527975hg38UCSC Ensembl
Innerchr8:39335536..39385494hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3849959
hg1949959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1176n145
Supporting Variantsnssv14085288
Samplessample165
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116390
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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