A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117612



Internal ID21300878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36192097..36197090hg38UCSC Ensembl
Innerchr14:36661303..36666296hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg384994
hg194994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv323n145
Supporting Variantsnssv14095399
Samplessample157
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117612
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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