A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095096



Internal ID21283749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:63852236..63855792hg38UCSC Ensembl
Innerchr14:64318954..64322510hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg383557
hg193557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111633
Supporting Variants
Samplessample349
Known GenesSYNE2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095096
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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