A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113611



Internal ID21296877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75124273..75128148hg38UCSC Ensembl
Innerchr13:75698410..75702285hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg383876
hg193876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094444
Samplessample71
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113611
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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