A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105541



Internal ID21288095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189646772..189653058hg38UCSC Ensembl
Innerchr3:189364561..189370847hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg386287
hg196287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114208
Supporting Variants
Samplessample411
Known GenesTP63
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105541
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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