A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114180



Internal ID21297446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163139554..163233298hg38UCSC Ensembl
Innerchr3:162857342..162951086hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3893745
hg1993745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv819n145
Supporting Variantsnssv14108037
Samplessample324
Known GenesCT64
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114180
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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