A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094968



Internal ID21287539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:103690589..103707008hg38UCSC Ensembl
Innerchr4:104611746..104628165hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3816420
hg1916420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112135
Supporting Variants
Samplessample402
Known GenesTACR3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094968
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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