A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105312



Internal ID21293345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4079460..4128601hg38UCSC Ensembl
Innerchr3:4121144..4170285hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3849142
hg1949142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115388
Supporting Variants
Samplessample99
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105312
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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