A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113313



Internal ID21296579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:28607482..28612661hg38UCSC Ensembl
Innerchr13:29181619..29186798hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg385180
hg195180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095630
Samplessample166
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113313
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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