A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107165



Internal ID21267194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:53208491..53223342hg38UCSC Ensembl
Innerchr4:54074658..54089509hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3814852
hg1914852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114615
Supporting Variants
Samplessample11
Known GenesSCFD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107165
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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