A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115027



Internal ID21298293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:141211606..141224513hg38UCSC Ensembl
Innerchr5:140591178..140604085hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3812908
hg1912908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109178
Samplessample265
Known GenesPCDHB12, PCDHB13, PCDHB14
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115027
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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