A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113136



Internal ID21296402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172968487..172973001hg38UCSC Ensembl
Innerchr3:172686277..172690791hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg384515
hg194515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108565
Samplessample359
Known GenesSPATA16
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113136
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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