A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589988



Internal ID16377397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26391122..26404443hg38UCSC Ensembl
Innerchr3:26432613..26445934hg19UCSC Ensembl
Innerchr3:26407617..26420938hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3813322
hg1913322
hg1813322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8270n54
Supporting Variantsnssv960343, nssv960341, nssv960342, nssv960340
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589988
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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