A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588868



Internal ID16029591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25737808..25778201hg38UCSC Ensembl
Innerchr22:26133775..26174168hg19UCSC Ensembl
Innerchr22:24463775..24504168hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3840394
hg1940394
hg1840394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954547
Samples
Known GenesMYO18B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588868
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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