A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112679



Internal ID21295945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:33245155..33251802hg38UCSC Ensembl
Innerchr13:33819292..33825939hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg386648
hg196648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094530
Samplessample115
Known GenesSTARD13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112679
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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