A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110289



Internal ID21293555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81389751..81402598hg38UCSC Ensembl
Innerchr17:79363551..79376398hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3812848
hg1912848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097745
Samplessample263
Known GenesBAHCC1, MIR4740
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110289
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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