A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110212



Internal ID21293478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:99005301..99007505hg38UCSC Ensembl
Innerchr1:99470857..99473061hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg382205
hg192205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091396
Samplessample289
Known GenesLOC100129620
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110212
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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