A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114960



Internal ID21298226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:84570504..84576893hg38UCSC Ensembl
Innerchr1:85036187..85042576hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg386390
hg196390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086686
Samplessample206
Known GenesCTBS
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114960
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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