A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584225



Internal ID16371634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:203316609..203326381hg38UCSC Ensembl
Innerchr2:204181332..204191104hg19UCSC Ensembl
Innerchr2:203889577..203899349hg18UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg389773
hg199773
hg189773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7261n54
Supporting Variantsnssv930568, nssv930569
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584225
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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