A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584106



Internal ID16371515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194444424..194521287hg38UCSC Ensembl
Innerchr2:195309148..195386011hg19UCSC Ensembl
Innerchr2:195017393..195094256hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3876864
hg1976864
hg1876864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7241n54
Supporting Variantsnssv930177
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584106
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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