A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111654



Internal ID21294920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:161240276..161246220hg38UCSC Ensembl
Innerchr2:162096787..162102731hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg385945
hg195945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104623
Samplessample138
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111654
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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