A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086686



Internal ID21274386
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 StatusS
Merged Variantsnsv3114960
Supporting Variants
Samplessample206
Known GenesCTBS
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086686
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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