A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094264



Internal ID21267043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:25484540..25489766hg38UCSC Ensembl
Innerchr14:25953746..25958972hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385227
hg195227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112161
Supporting Variants
Samplessample107
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094264
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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