A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102154



Internal ID21284438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45869198..45978669hg38UCSC Ensembl
Innerchr21:47289112..47398583hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38109472
hg19109472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114374
Supporting Variants
Samplessample360
Known GenesPCBP3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102154
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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