A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589035



Internal ID16376444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:40195244..40201049hg38UCSC Ensembl
Innerchr22:40591248..40597053hg19UCSC Ensembl
Innerchr22:38921194..38926999hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385806
hg195806
hg185806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957066
Samples
Known GenesTNRC6B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589035
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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