A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584108



Internal ID16371517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194451285..194521287hg38UCSC Ensembl
Innerchr2:195316009..195386011hg19UCSC Ensembl
Innerchr2:195024254..195094256hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3870003
hg1970003
hg1870003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7241n54
Supporting Variantsnssv930179, nssv930180
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584108
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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