A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102575



Internal ID21280514
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 StatusS
Merged Variantsnsv3111138
Supporting Variants
Samplessample3
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102575
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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