A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112709



Internal ID21295975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108089579..108093877hg38UCSC Ensembl
Innerchr3:107808426..107812724hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg384299
hg194299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108510
Samplessample348
Known GenesCD47
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112709
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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