A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111138



Internal ID21294404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26053191..26055330hg38UCSC Ensembl
Innerchr22:26449157..26451296hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382140
hg192140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104012, nssv14102579, nssv14102575
Samplessample3, sample4, sample419
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111138
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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