A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116562



Internal ID21299828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26621121..26626220hg38UCSC Ensembl
Innerchr3:26662612..26667711hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106367
Samplessample138
Known GenesLRRC3B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116562
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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