A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588879



Internal ID16376288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:28144504..28357845hg38UCSC Ensembl
Innerchr22:28540492..28753833hg19UCSC Ensembl
Innerchr22:26870492..27083833hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38213342
hg19213342
hg18213342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954555
Samples
Known GenesMIR548AM, TTC28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588879
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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