A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116226



Internal ID21299492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67567036..67573125hg38UCSC Ensembl
Innerchr17:65563152..65569241hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg386090
hg196090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098792
Samplessample99
Known GenesPITPNC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116226
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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