A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111823



Internal ID21295089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:168112271..168115599hg38UCSC Ensembl
Innerchr3:167830059..167833387hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg383329
hg193329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103496
Samplessample25
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111823
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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