A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111066



Internal ID21294332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39411668..39528445hg38UCSC Ensembl
Innerchr8:39269187..39385964hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38116778
hg19116778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1174n145
Supporting Variantsnssv14085317
Samplessample171
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111066
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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