A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111731



Internal ID21294997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68475301..68530194hg38UCSC Ensembl
Innerchr4:69341019..69395912hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3854894
hg1954894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv886n145
Supporting Variantsnssv14107640
Samplessample91
Known GenesTMPRSS11E
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111731
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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