A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110409



Internal ID21293675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:182792730..182795833hg38UCSC Ensembl
Innerchr3:182510518..182513621hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg383104
hg193104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106646
Samplessample182
Known GenesATP11B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110409
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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