A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118301



Internal ID21301567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85634543..85689499hg38UCSC Ensembl
Innerchr13:86208678..86263634hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3854957
hg1954957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095797
Samplessample250
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118301
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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