A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115306



Internal ID21298572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:12019930..12024784hg38UCSC Ensembl
Innerchr17:11923247..11928101hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384855
hg194855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098624
Samplessample378
Known GenesMAP2K4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115306
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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