A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115993



Internal ID21299259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:22797406..23390999hg38UCSC Ensembl
Innerchr5:22797515..23391108hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg38593594
hg19593594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096724
Samplessample19
Known GenesCDH12
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115993
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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