A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115530



Internal ID21298796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:85884615..85892647hg38UCSC Ensembl
Innerchr2:86111738..86119770hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg388033
hg198033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106031
Samplessample289
Known GenesST3GAL5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115530
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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