A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115561



Internal ID21298827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112097755..112151732hg38UCSC Ensembl
Innerchr3:111816602..111870579hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3853978
hg1953978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104366
Samplessample59
Known GenesC3orf52, GCSAM, MIR567, SLC9C1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115561
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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