A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588880



Internal ID16029603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:28411289..28605801hg38UCSC Ensembl
Innerchr22:28807277..29001789hg19UCSC Ensembl
Innerchr22:27137277..27331789hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38194513
hg19194513
hg18194513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954556
Samples
Known GenesMIR5739, TTC28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588880
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer