A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588033



Internal ID16375442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15310288..15409947hg38UCSC Ensembl
Innerchr22:16568016..16667675hg19UCSC Ensembl
Innerchr22:14948016..15047675hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3899660
hg1999660
hg1899660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7939n54
Supporting Variantsnssv949461
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588033
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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