A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589036



Internal ID16376445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:40195244..40203627hg38UCSC Ensembl
Innerchr22:40591248..40599631hg19UCSC Ensembl
Innerchr22:38921194..38929577hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg388384
hg198384
hg188384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957069, nssv957067, nssv957068
Samples
Known GenesTNRC6B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589036
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer