A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111002



Internal ID21294268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:58135311..58191391hg38UCSC Ensembl
Innerchr13:58709445..58765525hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3856081
hg1956081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094389, nssv14094431
Samplessample66, sample47
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111002
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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