A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113832



Internal ID21297098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67423128..67430121hg38UCSC Ensembl
Innerchr17:65419244..65426237hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg386994
hg196994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098652
Samplessample391
Known GenesPITPNC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113832
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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