A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111481



Internal ID21294747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41373732..41378722hg38UCSC Ensembl
Innerchr13:41947868..41952858hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg384991
hg194991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094363
Samplessample36
Known GenesNAA16
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111481
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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