A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584094



Internal ID16371503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194311489..194501360hg38UCSC Ensembl
Innerchr2:195176213..195366084hg19UCSC Ensembl
Innerchr2:194884458..195074329hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38189872
hg19189872
hg18189872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv930164, nssv930163
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584094
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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