A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588008



Internal ID16028731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15408473..15919545hg38UCSC Ensembl
Innerchr22:16058463..16569490hg19UCSC Ensembl
Innerchr22:14438463..14949490hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38511073
hg19511028
hg18511028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7934n54
Supporting Variantsnssv949426
Samples
Known GenesBMS1P17, BMS1P18, OR11H1, POTEH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588008
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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