A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115885



Internal ID21299151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148073867..148076741hg38UCSC Ensembl
Innerchr6:148395003..148397877hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382875
hg192875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1075n145
Supporting Variantsnssv14087828
Samplessample250
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115885
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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