A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118072



Internal ID21301338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:54122553..54132485hg38UCSC Ensembl
Innerchr14:54589271..54599203hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg389933
hg199933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093962
Samplessample287
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118072
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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