A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589010



Internal ID16029733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38864027..38895853hg38UCSC Ensembl
Innerchr22:39260032..39291858hg19UCSC Ensembl
Innerchr22:37589978..37621804hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3831827
hg1931827
hg1831827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv956722
Samples
Known GenesCBX6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589010
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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