A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117712



Internal ID21300978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:165356223..165358233hg38UCSC Ensembl
Innerchr4:166277375..166279385hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382011
hg192011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094711, nssv14092137
Samplessample218, sample360
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117712
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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