A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584883



Internal ID16372292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240869364..240879320hg38UCSC Ensembl
Innerchr2:241808781..241818737hg19UCSC Ensembl
Innerchr2:241457454..241467410hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg389957
hg199957
hg189957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7374n54
Supporting Variantsnssv934085
Samples
Known GenesAGXT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584883
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