A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115456



Internal ID21298722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13748078..13751850hg38UCSC Ensembl
Innerchr1:14074573..14078345hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg383773
hg193773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085858
Samplessample216
Known GenesPRDM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115456
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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