A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111449



Internal ID21294715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45158685..45165138hg38UCSC Ensembl
Innerchr22:45554566..45561019hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg386454
hg196454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102807
Samplessample120
Known GenesLOC100506714, NUP50
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111449
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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