A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113185



Internal ID21296451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67422122..67424275hg38UCSC Ensembl
Innerchr17:65418238..65420391hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098656
Samplessample392
Known GenesPITPNC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113185
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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