A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110573



Internal ID21293839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:58636337..58638994hg38UCSC Ensembl
Innerchr14:59103055..59105712hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg382658
hg192658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093966
Samplessample289
Known GenesDACT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110573
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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