A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094296



Internal ID21267745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103513828..103553175hg38UCSC Ensembl
Innerchr14:103980165..104019512hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3839348
hg1939348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113040
Supporting Variants
Samplessample116
Known GenesCKB, TRMT61A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094296
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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