A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112590



Internal ID21295856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40323374..40342208hg38UCSC Ensembl
Innerchr14:40792578..40811412hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3818835
hg1918835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095210
Samplessample400
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112590
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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