A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113969



Internal ID21297235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197700330..197705133hg38UCSC Ensembl
Innerchr3:197427201..197432004hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg384804
hg194804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108585
Samplessample362
Known GenesKIAA0226
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113969
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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