A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116468



Internal ID21299734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169063796..169069166hg38UCSC Ensembl
Innerchr6:169463891..169469261hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg385371
hg195371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1088n145
Supporting Variantsnssv14083761
Samplessample78
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116468
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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