A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111038



Internal ID21294304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52307527..52359753hg38UCSC Ensembl
Innerchr13:52881662..52933888hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3852227
hg1952227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095872
Samplessample302
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111038
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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