A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095215



Internal ID21287700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87304126..87310732hg38UCSC Ensembl
Innerchr14:87770470..87777076hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg386607
hg196607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111784
Supporting Variants
Samplessample405
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095215
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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