A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111817



Internal ID21295083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140065085..140070644hg38UCSC Ensembl
Innerchr6:140386222..140391781hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg385560
hg195560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1074n145
Supporting Variantsnssv14086545, nssv14083000, nssv14084489, nssv14086432, nssv14083779, nssv14083714, nssv14086348, nssv14087576, nssv14082850, nssv14083845, nssv14089215
Samplessample98, sample11, sample64, sample82, sample125, sample165, sample143, sample186, sample390, sample332, sample286
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111817
Frequency
Sample Size467
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer