A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589276



Internal ID16376685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188773..192626hg38UCSC Ensembl
Innerchr3:230456..234309hg19UCSC Ensembl
Innerchr3:205456..209309hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg383854
hg193854
hg183854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8149n54
Supporting Variantsnssv957784, nssv957785, nssv957783
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589276
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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