A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111238



Internal ID21294504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:16842664..16855648hg38UCSC Ensembl
Innerchr2:17023931..17036915hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3812985
hg1912985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103205, nssv14106247
Samplessample76, sample335
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111238
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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