A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094130



Internal ID21290054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36681155..36685369hg38UCSC Ensembl
Innerchr14:37150360..37154574hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg384215
hg194215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112131
Supporting Variants
Samplessample54
Known GenesSLC25A21
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094130
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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