A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115602



Internal ID21298868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:87329363..87331107hg38UCSC Ensembl
Innerchr1:87795046..87796790hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381745
hg191745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084458
Samplessample14
Known GenesLMO4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115602
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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