A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095537



Internal ID21274525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99479283..99483104hg38UCSC Ensembl
Innerchr14:99945620..99949441hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383822
hg193822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110495
Supporting Variants
Samplessample208
Known GenesCCNK, SETD3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095537
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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