A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111016



Internal ID21294282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:171149871..171152027hg38UCSC Ensembl
Innerchr1:171119010..171121166hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg382157
hg192157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv85n145
Supporting Variantsnssv14091889
Samplessample277
Known GenesFMO6P
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111016
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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