A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112188



Internal ID21295454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16108901..16114129hg38UCSC Ensembl
Innerchr4:16110524..16115752hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg385229
hg195229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv859n145
Supporting Variantsnssv14092133, nssv14089345, nssv14094828
Samplessample379, sample218, sample118
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112188
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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