A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114269



Internal ID21297535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27890077..27896174hg38UCSC Ensembl
Innerchr17:26217103..26223200hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg386098
hg196098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098449
Samplessample300
Known GenesLYRM9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114269
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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