A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113862



Internal ID21297128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189647214..189653058hg38UCSC Ensembl
Innerchr3:189365003..189370847hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg385845
hg195845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv836n145
Supporting Variantsnssv14108333, nssv14104311, nssv14104520, nssv14106478
Samplessample50, sample153, sample236, sample86
Known GenesTP63
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113862
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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