A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118054



Internal ID21301320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78811288..78814066hg38UCSC Ensembl
Innerchr6:79521005..79523783hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382779
hg192779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1050n145
Supporting Variantsnssv14083867, nssv14083550, nssv14083568
Samplessample396, sample32, sample35
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118054
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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