A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116020



Internal ID21299286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39484797..39499344hg38UCSC Ensembl
Innerchr8:39342316..39356863hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3814548
hg1914548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1177n145
Supporting Variantsnssv14085811
Samplessample21
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116020
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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