A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112760



Internal ID21296026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94472228..94492666hg38UCSC Ensembl
Innerchr1:94937784..94958222hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3820439
hg1920439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107495
Samplessample105
Known GenesABCD3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112760
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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