A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111096



Internal ID21294362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45139803..45144715hg38UCSC Ensembl
Innerchr22:45535684..45540596hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg384913
hg194913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv737n145
Supporting Variantsnssv14102750
Samplessample98
Known GenesLOC100506714
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111096
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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