A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118142



Internal ID21301408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98080687..98083044hg38UCSC Ensembl
Innerchr3:97799531..97801888hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg382358
hg192358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108238
Samplessample221
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118142
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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