A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110646



Internal ID21293912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:29554306..29561163hg38UCSC Ensembl
Innerchr13:30128443..30135300hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg386858
hg196858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094591
Samplessample146
Known GenesSLC7A1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110646
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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