A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084314



Internal ID21270268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2354378..2359543hg38UCSC Ensembl
Innerchr7:2394013..2399178hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg385166
hg195166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114767
Supporting Variants
Samplessample149
Known GenesEIF3B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084314
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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