A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588891



Internal ID16376300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:31024156..31032867hg38UCSC Ensembl
Innerchr22:31420142..31428853hg19UCSC Ensembl
Innerchr22:29750142..29758853hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg388712
hg198712
hg188712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954604
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588891
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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