A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588179



Internal ID16028902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:18890274..19039100hg38UCSC Ensembl
Innerchr22:18877787..19026613hg19UCSC Ensembl
Innerchr22:17257787..17406613hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38148827
hg19148827
hg18148827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7969n54
Supporting Variantsnssv951650, nssv951648, nssv951649, nssv951651
Samples
Known GenesDGCR10, DGCR2, DGCR5, DGCR6, DGCR9, PRODH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588179
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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