A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095399



Internal ID21270958
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 StatusS
Merged Variantsnsv3117612
Supporting Variants
Samplessample157
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095399
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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