A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584722



Internal ID16025445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:236174434..236247906hg38UCSC Ensembl
Innerchr2:237083077..237156549hg19UCSC Ensembl
Innerchr2:236747816..236821288hg18UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3873473
hg1973473
hg1873473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7342n54
Supporting Variantsnssv933653
Samples
Known GenesASB18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584722
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