A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112359



Internal ID21295625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85740216..85745317hg38UCSC Ensembl
Innerchr9:88355131..88360232hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088141
Samplessample360
Known GenesAGTPBP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112359
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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